Find where to buy products from suppliers in the USA, including: distributors, industrial manufacturers in America, bulk supplies and wholesalers of raw ingredients & finished goods.
Search for products or services, then visit the American suppliers website for prices, SDS or more information. You can also view suppliers in Australia, NZ or the UK.
| Product | Description | |
|---|---|---|
| (+)-1-(1-Naphthyl)ethylamine | (+)-1-(1-Naphthyl)ethylamine ((+)-1-(1-NEA)) is a chiral modifier used to introduce enantioselectivity in catalytic hydrogenation reactions. 1-NEA can undergo H-D exchange with D2 in solution to form N D bonds. That is, 1-NEA can complete Pt surface adsorption and protonation through amine N atoms, indicating that NEA molecules have the potential to impart enantioselectivity to Pt hydrogenation catalysts [1]. Uses: Scientific research. Group: Biochemical assay reagents. CAS No. 3886-70-2. Pack Sizes: 25 g; 50 g; 100 g. Product ID: HY-75070. |  |
| 1,2,3,4-Tetrahydro-1-napthol | 1,2,3,4-Tetrahydro-1-napthol is a chemical reagent used as a catalyst in hydrogenation reactions. Group: Biochemicals. Grades: Highly Purified. CAS No. 529-33-9. Pack Sizes: 1g, 5g. Molecular Formula: C10H20O, Molecular Weight: 148.199999999999. US Biological Life Sciences. |  Worldwide |
| (-)-1,2-Bis((2R,5R)-2,5-dimethylphospholano)benzene(1,5-cyclooctadiene)rhodium(I) tetrafluoroborate, 98+% (R,R)-Me-DUPHOS-Rh | (-)-1,2-Bis((2R,5R)-2,5-dimethylphospholano)benzene(1,5-cyclooctadiene)rhodium(I) tetrafluoroborate, 98+% (R,R)-Me-DUPHOS-Rh. Uses: The duphos family of catalysts is highly efficient for the asymmetric hydrogenation of various substituted acetamidoacrylates and enol acetates yielding products of high enantiomeric excesses. efficient ligand for the asymmetric hydrogenation of tetrasubstituted enamides. forms superior catalysts for asymmetric reductive aminations. catalyst used for the asymmetric hydrogenation of enol phosphon. Additional or Alternative Names: 210057-23-1;MFCD01862466;057B231;(-)-1,2-Bis[(2R,5R)-dimethylphospholano]benzene(cyclooCtadiene)rhodium(I) tetrafluoroborate;1,2-Bis[(2R,5R)-2,5-dimethylphospholano]benzene(cyclooctadiene)rhodium(I)tetrafluoroborate;(-)-1,2-Bis((2R,5R)-2,5-dimethylphospholano)benzene(cyclooctadiene)rhodium (I) tetrafluoroborate;(-)-1,2-Bis((2R,5R)-2,5-dimethylphospholano)benzene(cyclooctadiene)rhodium(I) tetrafluo. Product Category: Rhodium series of catalysts. CAS No. 210057-23-1. Molecular formula: C26H40BF4P2Rh-. Mole weight: 604.263g/mol. IUPACName: cycloocta-1,5-diene;(2R,5R)-1-[2-[(2R,5R)-2,5-dimethylphospholan-1-yl]phenyl]-2,5-dimethylphospholane;rhodium;tetrafluoroborate. Canonical SMILES: [B-](F)(F)(F)F.CC1CCC(P1C2=CC=CC=C2P3C(CCC3C)C)C.C1CC=CCCC=C1.[Rh]. ECNumber: 446 |  |
| (+)-1,2-Bis((2S,5S)-2,5-dimethylphospholano)benzene(1,5-cyclooctadiene)rhodium(I) tetrafluoroborate, 98+% (S,S)-Me-DUPHOS-Rh | (+)-1,2-Bis((2S,5S)-2,5-dimethylphospholano)benzene(1,5-cyclooctadiene)rhodium(I) tetrafluoroborate, 98+% (S,S)-Me-DUPHOS-Rh. Uses: The duphos family of catalysts is highly efficient for the asymmetric hydrogenation of various substituted acetamidoacrylates and enol acetates yielding products of high enantiomeric excesses. efficient ligand for the asymmetric hydrogenation of tetrasubstituted enamides. forms superior catalysts for asymmetric reductive aminations. catalyst used for the asymmetric hydrogenation of enol phosphon. Additional or Alternative Names: (+)-1,2-Bis((2S,5S)-2,5-dimethylphospholano)benzene(cyclooctadiene)Rh(I)tetrafluoroborate; (2R,5R)-1-[2-[(2R,5R)-2,5-dimethylphospholan-1-yl]phenyl]-2,5-dimethylphospholane; MFCD01862467; 205064-10-4; AC1MC1E8. Product Category: Rhodium series of catalysts. CAS No. 205064-10-4. Molecular formula: C26H40BF4P2Rh-. Mole weight: 604.263g/mol. IUPACName: cycloocta-1,5-diene;(2S,5S)-1-[2-[(2S,5S)-2,5-dimethylphospholan-1-yl]phenyl]-2,5-dimethylphospholane;rhodium;tetrafluoroborate. Canonical SMILES: [B-](F)(F)(F)F.CC1CCC(P1C2=CC=CC=C2P3C(CCC3C)C)C.C1CC=CCCC=C1.[Rh]. Product ID: ACM205064104. Alfa Chemistry ISO 9001:2015 Certified. | |
| 1, 2-Bis [ (s, s) -2, 5-diphenylphospholano] ethane- (1, 5-cycloocta-diene) rhodium (I) tetrafluoroborate | An asymmetric hydrogenation catalyst. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| 1,3-Bis(2,6-Diisopropylphenyl)-4,5-Dihydroimidazolium Tetrafluoroborate | 1,3-Bis(2,6-Diisopropylphenyl)-4,5-Dihydroimidazolium Tetrafluoroborate. Uses: In-situ deprotonation leads to metal carbene species which acts as a catalyst in a variety of c-c and c-n bond forming reactions. ligand used in the nickel or palladium-catalyzed coupling of aryl chlorides and amines. ligand used for the palladium-catalyzed arylation of esters and amides. ligand used for the palladium-catalyzed intermolecular amination of csp3-h bonds. ligand used for the nickel-catalyzed hydrogenation of olefins. Additional or Alternative Names: 1,3-Bis(2,6-Diisopropylphenyl)-4,5-Dihydro-1H-Imidazol-3-Ium Tetrafluoroborate. Product Category: Organic Phosphine Compounds. Appearance: White powder. CAS No. 282109-83-5. Molecular formula: C27H39BF4N2. Mole weight: 478.4. Purity: 0.98. IUPACName: 1,3-bis[2,6-di(propan-2-yl)phenyl]-4,5-dihydroimidazol-1-ium;tetrafluoroborate. Canonical SMILES: [B-](F)(F)(F)F.CC(C)C1=C(C(=CC=C1)C(C)C)N2CC[N+](=C2)C3=C(C=CC=C3C(C)C)C(C)C. Product ID: ACM282109835-1. Alfa Chemistry ISO 9001:2015 Certified. | |
| 1- (3-Ethoxy-4-methoxy-phenyl) -2-methane sulfonylethylamine | 1- (3-Ethoxy-4-methoxy-phenyl) -2-methane sulfonylethylamine is used in the enantioselective synthesis of Apremilast (A729700) aminosulfone using catalytic asymetric hydrogenation. Apremilast EP Impurity H. Group: Biochemicals. Grades: Highly Purified. CAS No. 253168-94-4. Pack Sizes: 250mg, 1g. Molecular Formula: C12H19NO4S, Molecular Weight: 273.35. US Biological Life Sciences. | Worldwide |
| (-)-(14α)-Dihydrovinpocetine-d5 | (-)-(14α)-Dihydrovinpocetine-d5 is labelled (-)-Dihydroapovincaminic Acid Ethyl Ester (D448350), a chiral modifier in enantioselective heterogeneous catalytic hydrogenations. It is also structurally related to Vinpocetine (V332500), a Vasodilator (cerebral). Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 1mg. Molecular Formula: C22H23D5N2O2, Molecular Weight: 357.5. US Biological Life Sciences. | Worldwide |
| (+)-(14 β)-Dihydrovinpocetine | (+)-(14 β)-Dihydrovinpocetine is a stereoisomer of (-)-Dihydroapovincaminic Acid Ethyl Ester (D448350), a chiral modifier in enantioselective heterogeneous catalytic hydrogenations. It is also structurally related to Vinpocetine (V332500), a Vasodilator (cerebral). Group: Biochemicals. Grades: Highly Purified. CAS No. 57517-54-1. Pack Sizes: 2.5mg, 25mg. Molecular Formula: C22H28N2O2, Molecular Weight: 352.47. US Biological Life Sciences. | Worldwide |
| (+)-(14 β)-Dihydrovinpocetine-d5 | (+)-(14 β)-Dihydrovinpocetine-d5 is labelled (+)-(14 β)-Dihydrovinpocetine (D448385) which is a stereoisomer of (-)-Dihydroapovincaminic Acid Ethyl Ester (D448350), a chiral modifier in enantioselective heterogeneous catalytic hydrogenations. It is also structurally related to Vinpocetine (V332500), a Vasodilator (cerebral). Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 1mg, 10mg. Molecular Formula: C22H23D5N2O2, Molecular Weight: 357.5. US Biological Life Sciences. | Worldwide |
| 16-Dehydroprogesterone | 16-Dehydroprogesterone is used in the direct organocatalytic stereoselective transfer hydrogenation of conjugated olefins of steroids. 16-Dehydroprogesterone is a form of Progesterone (P755900), a steroid hormone produced by the corpus luteum that induces maturation and secretory activity of the uterine endothelium; suppresses ovulation. Progesterone is implicated in the etiology of breast cancer. Group: Biochemicals. Grades: Highly Purified. CAS No. 1096-38-4. Pack Sizes: 50mg, 100mg. Molecular Formula: C21H28O2. US Biological Life Sciences. | Worldwide |
| 1,6-Hexanediol | 1,6-Hexanediol is a saturated straight-chain diol, colorless liquid at room temperature, soluble in water. Industrially, 1,6-hexanediol can be synthesized by hydrogenation of adipic acid or its esters. It is usually prepared in the laboratory by the reduction of adipic acid with lithium aluminum hydride. Uses: 1,6-hexanediol can be used for a variety of s such as: a structure-directing agent for the synthesis of zsm-5 zeolite a solvent for titanium tetraisopropoxide to form titanium oxide (tio2) nanocrystals a phase change material in combination with lauric acid for thermal energy storage s. Group: 3d printing materials monomers. Alternative Names: Hexamethylene glycol. CAS No. 629-11-8. Pack Sizes: Packaging 50 g in poly bottle. Product ID: hexane-1,6-diol. Molecular formula: 118.17. Mole weight: HO(CH2)6OH. OCCCCCCO. 1S/C6H14O2/c7-5-3-1-2-4-6-8/h7-8H, 1-6H2. XXMIOPMDWAUFGU-UHFFFAOYSA-N. ≥ 97%. |  |
| 1, 8-Dinitropyrene | A derivative of Pyrene. Pyrene is a polycyclic aromatic hydrocarbon consisting of four fused benzene rings, resulting in a flat aromatic system. Pyrene occurs in coal tar. Also obtained by the destructive hydrogenation of hard coal. Grade: > 95%. CAS No. 42397-65-9. Molecular formula: C16H8N2O4. Mole weight: 292.25. |  |
| 1-Aminopyrene-d9 | 1-Pyren-2,3,4,5,6,7,8,9,10-d9-amine is derived from Pyrene-d10 (P849002), which is labelled Pyrene. Occurs in coal tar. Also obtained by the destructive hydrogenation of hard coal. Group: Biochemicals. Grades: Highly Purified. CAS No. 128008-86-6. Pack Sizes: 1mg, 2.5mg. Molecular Formula: C16H2D9N. US Biological Life Sciences. | Worldwide |
| 1-Butyne-3,3,4,4,4-d5 | 1-Butyne-3,3,4,4,4-d5 is deuterium labelled 1-Butyne. 1-Butyne can be utilized for stereocontrolled synthesis such as controlled hydrogenation of terminal alkynes. It can also be used to synthesize polyene natural products by iterative cross coupling. Group: Biochemicals. Grades: Highly Purified. CAS No. 60173-50-4. Pack Sizes: 100mL, 250mL. Molecular Formula: C4HD5, Molecular Weight: 59.12. US Biological Life Sciences. | Worldwide |
| 1-Cyclohexenylalde hyde1192-88-7 | 1-Cyclohexenylaldehyde can be used as reactant/reagent in chemoselective synthesis of aliphatic alcohols via NSS-ruthenium complex-catalyzed hydrogenation of α, β-unsaturated carbonyl compounds. Group: Biochemicals. Grades: Highly Purified. CAS No. 1192-88-7. Pack Sizes: 50mg, 250mg. Molecular Formula: C7H10O, Molecular Weight: 110.15. US Biological Life Sciences. | Worldwide |
| 1-Nitropyrene-d9 | 1-Nitropyrene-d9 is a labelled isotope of 1-Nitropyrene (N519950), which is the most abundant nitropolycylcic aromatic hydrocarbon found in exhaust from diesel engines with potent carcinogenic and mutagenic properties. It is also an intermediate in synthesizing 1-Aminopyrene-d9 (A629287), which is derived from Pyrene-d10 (P849002), which is labelled Pyrene. Occurs in coal tar. Also obtained by the destructive hydrogenation of hard coal. Group: Biochemicals. Grades: Highly Purified. CAS No. 93487-20-8. Pack Sizes: 500ug, 1mg. Molecular Formula: C16D9NO2. US Biological Life Sciences. | Worldwide |
| 1-Tetradecyne | 1-Tetradecyne is used in addition reactions of alkynes like hydrogenation, halogenation, hydrohalogenation, hydration reactions and others. Group: Biochemicals. Grades: Highly Purified. CAS No. 765-10-6. Pack Sizes: 1ml, 2.5ml. Molecular Formula: C14H26, Molecular Weight: 194.36. US Biological Life Sciences. | Worldwide |
| [2,2'-Bis(diphenylphosphino)-1,1'-binaphthalene]chloro(p-cymene)ruthenium Chloride | [2,2'-Bis(diphenylphosphino)-1,1'-binaphthalene]chloro(p-cymene)ruthenium Chloride is used as a catalyst in the asymmetric synthesis of UK 370106 (U700620); an MMP-3 inhibitor. It is also highly effective in the hydrogenation of 2-(6'-methoxy-2'-naphthyl)propenoic acid and β-ketoesters. Group: Biochemicals. Grades: Highly Purified. CAS No. 130004-33-0. Pack Sizes: 100mg, 250mg. Molecular Formula: C54H46Cl2P2Ru. US Biological Life Sciences. | Worldwide |
| 2,2'-Bis(diphenylphosphino)biphenyl | 2,2'-Bis(diphenylphosphino)biphenyl. Uses: Supporting ligand in a chiral diamine-ruthenium system for the enantioselective hydrogenation of ketones. useful ligand for palladium-catalyzed amination and kumada cross-coupling reactions useful ligand for palladium-catalyzed synthesis of butatrenes. useful ligand for iridium-catalyzed c-c cross-coupling of allenes with primary alcohols via transfer hydrogenation. useful ligand for iridium-catalyzed c-c cross-coupling of dienes with primary alcohols via transfer hydrogenation. useful ligand for iridium-catalyzed c-c cross-coupling of allylic gem-dicarboxylates with aldehydes via transfer hydrogenation. useful ligand for the palladium-catalyzed synthesis of chiral allenylsilanes. ruthenium-catalyzed synthesis of indoles. ruthenium-catalyzed oxidative cyclization. rhodium-catalyzed boron arylation. Additional or Alternative Names: BIPHEP; MFCD03094574; AKOS015911364; DB-009479; 1,1'-[[1,1'-BIPHENYL]-2,2'-DIYL]BIS[1,1-DIPHENYL]-PHOSPHINE; CTK3J1519; SCHEMBL1120987; 2,2'-Bis(diphenylphosphino)biphenyl; 2,2'-bis(diphenylphosphanyl)-1,1'-biphenyl; FT-0657577. Product Category: Organic Phosphine Compounds. CAS No. 84783-64-2. Molecular formula: C36H28P2. Mole weight: 522.568g/mol. IUPACName: [2-(2-diphenylphosphanylphenyl)phenyl]-diphenylphosphane. Canonical SMILES: C1=CC=C(C=C1)P(C2=CC=CC=C2)C3=CC=CC=C3C4=CC=CC=C4P(C5=CC=CC=C5)C6=CC=CC=C6. Product ID: ACM84783642. | |
| 2-(2-Chlorophenyl)ethanol | 2-(2-Chlorophenyl)ethanol is used in the triethylborane-catalyzed reduction of carbonyl functions to alcohols. 2-(2-Chlorophenyl)ethanol is also used in the preparation of alcohols via ruthenium-catalyzed hydrogenation of carboxylic acids. Group: Biochemicals. Grades: Highly Purified. CAS No. 19819-95-5. Pack Sizes: 1g, 5g. Molecular Formula: C8H9ClO, Molecular Weight: 156.61. US Biological Life Sciences. | Worldwide |
| 2-(4-Chlorobenzoyl)pyridine | 2-(4-Chlorobenzoyl)pyridine can be used as reactant/reagent in asymmetric transfer hydrogenation of aryl N-heteroaryl ketones catalyzed bifunctional oxo-tethered ruthenium complex. Group: Biochemicals. Grades: Highly Purified. CAS No. 6318-51-0. Pack Sizes: 1g, 5g. Molecular Formula: C12H8ClNO, Molecular Weight: 217.65. US Biological Life Sciences. | Worldwide |
| 2-Bromomesitylene | 2-Bromomesitylene is a useful synthetic intermediate. It is an intermediate used to prepare Hydrogen [4- [bis (2, 4, 6-trimethylphenyl) phosphino] -2, 3, 5, 6-tetrafluorophenyl] hydrobis (2, 3, 4, 5, 6-pentafluorophenyl) borate (H714510) which is a frustrated phosphonium borate for metal-free catalytic hydrogenation of imines. Group: Biochemicals. Grades: Highly Purified. CAS No. 576-83-0. Pack Sizes: 1g, 10g. Molecular Formula: C9H11Br, Molecular Weight: 199.09. US Biological Life Sciences. | Worldwide |
| 2-(Dicyclohexylphosphino)-N,N-diisopropyl-1H-indole-1-carboxamide | 2-(Dicyclohexylphosphino)-N,N-diisopropyl-1H-indole-1-carboxamide. Uses: Chloronorbornadienetriphenylphosphinerhodium (I) is versatile polymer-bound catalyst used for the selective hydrogenation of polyolefins. the supported rhodium catalyst exhibits similar selectivity to its homogeneous counterpart. in most cases, rhodium leaching is negligible. Additional or Alternative Names: SCHEMBL17513080;MFCD20257903;ZINC86032091;1067175-36-3;2-(Dicyclohexylphosphino)-N,N-bis(1-methylethyl)-1H-indole-1-carboxamide;2-(Dicyclohexylphosphino)-N,N-diisopropyl-1H-indole-1-carboxamide, 97%. Product Category: Heterocyclic Organic Compound. CAS No. 1067175-36-3. Molecular formula: C27H41N2OP. Mole weight: 440.612g/mol. IUPACName: 2-dicyclohexylphosphanyl-N,N-di(propan-2-yl)indole-1-carboxamide. Canonical SMILES: CC(C)N(C(C)C)C(=O)N1C2=CC=CC=C2C=C1P(C3CCCCC3)C4CCCCC4. Product ID: ACM1067175363. Alfa Chemistry ISO 9001:2015 Certified. | |
| [2-(Di-tert-butylphosphinomethyl)-6-(diethylaminomethyl)pyridine]carbonylchlorohydridoruthenium(II) | [2-(Di-tert-butylphosphinomethyl)-6-(diethylaminomethyl)pyridine]carbonylchlorohydridoruthenium(II). Uses: Ruthenium catalyst for the direct synthesis of amides from alcohols and primary amines. ruthenium catalyst for the hydrogenation of esters in high yields under mild pressure and neutral conditions. ruthenium catalyst for the dehydrogenative coupling of alcohols to form esters in high yields under neutral conditions. ruthenium catalyst for the synthesis of amides from esters and amines with liberation of hydrogen gas. ruthenium catalyst for the hydrogenation of 3-methyl-2-oxalidinone. Additional or Alternative Names: Carbonylchlorohydrido[6-(di-t-butylphosphinomethyl)-2-(N,N-diethylaminomethyl)pyridine]ruthenium(II);863971-62-4. Product Category: Ruthenium series catalysts. CAS No. 863971-62-4. Molecular formula: C20H37ClN2OPRu. Mole weight: 489.023g/mol. IUPACName: chlororuthenium;N-[[6-(ditert-butylphosphanylmethyl)pyridin-2-yl]methyl]-N-ethylethanamine;formaldehyde. Canonical SMILES: CCN(CC)CC1=NC(=CC=C1)CP(C(C)(C)C)C(C)(C)C.C=O.Cl[Ru]. Product ID: ACM863971624. Alfa Chemistry ISO 9001:2015 Certified. Categories: Milstein Catalyst Precursor. | |
| (2E, 4S) -5-[1, 1'-Biphenyl]-4-yl-4-[[ (1, 1-dimethylethoxy) carbonyl]amino]-2-methyl-2-pentenoic Acid | (2E, 4S) -5-[1, 1'-Biphenyl]-4-yl-4-[[ (1, 1-dimethylethoxy) carbonyl]amino]-2-methyl-2-pentenoic Acid was used in the study to process for preparation of biaryl-substituted 4-aminobutyric acids by hydrogenation of the corresponding alkenoates. Group: Biochemicals. Grades: Highly Purified. CAS No. 1015037-46-3. Pack Sizes: 10mg, 25mg. Molecular Formula: C23H27NO4, Molecular Weight: 381.46. US Biological Life Sciences. | Worldwide |
| 2-Hexanone | 2-Hexanone is used in various organic chemical syntheses. It is used in the synthesis of (+/-)-monomorine. It is also used in the preparation of alcohols by transfer hydrogenation of ketones. Group: Biochemicals. Alternative Names: 2-Oxohexane; Butyl Methyl Ketone; MBK; Methyl Butyl Ketone; Methyl n-Butyl Ketone; n-Butyl Methyl Ketone. Grades: Highly Purified. CAS No. 591-78-6. Pack Sizes: 25g. US Biological Life Sciences. | Worldwide |
| 2-Nitrodibenzothiophene | 2-Nitrodibenzothiophene is a nitrated polycyclic aromatic hydrocarbon (PAH). 2-Nitrodibenzothiophene is removed from coal by hydrogenation in Tetralin. Group: Biochemicals. Alternative Names: NSC 16062. Grades: Highly Purified. CAS No. 6639-36-7. Pack Sizes: 1g. US Biological Life Sciences. | Worldwide |
| (2R,3R)-(-)-2,3-Bis(diphenylphosphino)bicyclo[2.2.1]hept-5-ene(1,5-cyclooctadiene)rhodium(I) tetrafluoroborate, min. 97% (R,R)-NORPHOS-Rh | (2R,3R)-(-)-2,3-Bis(diphenylphosphino)bicyclo[2.2.1]hept-5-ene(1,5-cyclooctadiene)rhodium(I) tetrafluoroborate, min. 97% (R,R)-NORPHOS-Rh. Uses: Ligand used in the enantioselective rhodium catalyzed hydrogenation of α-dehydroaminoesters and enamides. ligand used in the enantioselective rhodium catalyzed hydroboration of cyclopropenes. ligand used in the asymmetric rhodium catalyzed cleavage of racemic 1,3-oxazolidines. Additional or Alternative Names: (R,R)-NORPHOS-Rh;MFCD09839137;(2R,3R)-(-)-2,3-bis(diphenylphosphino)bicyclo[2.2.1]hept-5-ene(1,5-cyclooctadiene)rhodium(I) tetrafluoroborate;(2R,3R)-(-)-2,3-Bis(diphenylphosphino)bicyclo[2.2.1]hept-5-ene(1,5-cyclooctadiene)rhodium(I)tetrafluoroborate;521272-85-5. Product Category: Heterocyclic Organic Compound. CAS No. 521272-85-5. Molecular formula: C39H40BF4P2Rh-. Mole weight: 760.406g/mol. IUPACName: (1Z,5Z)-cycloocta-1,5-diene;[(1S,2R,3R,4R)-3-diphenylphosphanyl-2-bicyclo[2.2.1]hept-5-enyl]-diphenylphosphane;rhodium;tetrafluoroborate. Canonical SMILES: [B-](F)(F)(F)F.C1CC=CCCC=C1.C1C2C=CC1C(C2P(C3=CC=CC=C3)C4=CC=CC=C4)P(C5=CC=CC=C5)C6=CC=CC=C6.[Rh]. Product ID: ACM521272855. Alfa Chemistry ISO 9001:2015 Certified. | |
| 3-Acetylpyridine Adenine Dinucleotide (APAD) | APAD is an NAD analog with higher oxidation potential than NAD. It can substitute for NAD as a hydrogen-accepting cofactor in many dehydrogenase reactions; e.g. lactate dehydrogenase from Toxoplasma, Clonorchis, and Plasmodium, bacterial lipoamide dehydrogenase, as well as mammalian dehydrogenases. It can also act as a proton acceptor in various transhydrogenation reactions with NADH or NADPH. Group: Biochemicals. Alternative Names: APAD; adenosine 5'-(trihydrogen diphosphate), P?5-ester with 3-acetyl-1- β -D-ribofuranosyl pyridinium , inner salt. Grades: Purified. CAS No. 86-08-8. Pack Sizes: 10mg, 25mg, 50mg, 100mg, 250mg. Molecular Formula: C22H28N6O14P2, Molecular Weight: 662.44. US Biological Life Sciences. | Worldwide |
| 3-Acetylpyridine-Adenine Dinucleotide, Oxidized (APAD) | 3-Acetylpyridine adenine dinucleotide is an NAD analog with higher oxidation potential than NAD. It can substitute for NAD as a hydrogen-accepting cofactor in many dehydrogenase reactions. For example lactate dehydrogenase from Toxoplasma, Clonorchis, and Plasmodium, bacterial lipoamide dehydrogenase, as well as mammalian dehydrogenases. This compound can also act as a proton acceptor in various transhydrogenation reactions with NADH or NADPH. Group: Coenzymes. Synonyms: aldehyde reductase; ADH; alcohol dehydrogenase (NAD); aliphatic alcohol dehydrogenase; ethanol dehydrogenase; NAD-dependent alcohol dehydrogenase; NA. Enzyme Commission Number: EC 1.1.1.1. CAS No. 1986-8-8. Purity: Determined by increase in absorbance at 363 nm on enzymatic reduction with ADH* at pH 10.0 > 92% *ADH = Alcohol dehydrogenase (Horse liver) (EC 1.1.1.1.). APAD. Mole weight: 662.44. Storage: Keep tightly stoppered in the dark below 5°C. Moisture will reduce the purity. For prolonged storage, keep below-20°C. aldehyde reductase; ADH; alcohol dehydrogenase (NAD); aliphatic alcohol dehydrogenase; ethanol dehydrogenase; NAD-dependent alcohol dehydrogenase; NAD-specific aromatic alcohol dehydrogenase; NADH-alcohol dehydrogenase; NADH-aldehyde dehydrogenase; primary alcohol dehydrogenase; yeast alcohol dehydrogenase; EC 1.1.1.1; APAD. Cat No: NATE-0077. |  |
| 3-Di-i-propylphosphino-2-(N,N-dimethylamino)-1H-indene(1,5-cyclooctadiene)iridium(I) hexafluorophosphate, min. 98% | 3-Di-i-propylphosphino-2-(N,N-dimethylamino)-1H-indene(1,5-cyclooctadiene)iridium(I) hexafluorophosphate, min. 98%. Uses: Zwitterionic hydrogenation, hydrosilylation and hydroboration catalyst soluble in non-polar solvents. Additional or Alternative Names: 870077-94-4;3-Di-i-propylphosphino-2-(N,N-dimethylamino)-1H-indene(1,5-cyclooctadiene)iridium(I) hexafluorophosphate;(1Z,5Z)-cycloocta-1,5-diene;3-di(propan-2-yl)phosphanyl-N,N-dimethyl-1H-inden-2-amine;iridium;hexafluorophosphate. Product Category: Iridium series of catalysts. CAS No. 870077-94-4. Molecular formula: C25H38F6IrNP2-. Mole weight: 720.741g/mol. IUPACName: cycloocta-1,5-diene;3-di(propan-2-yl)phosphanyl-N,N-dimethyl-1H-inden-2-amine;iridium;hexafluorophosphate. Canonical SMILES: CC(C)P(C1=C(CC2=CC=CC=C21)N(C)C)C(C)C.C1CC=CCCC=C1.F[P-](F)(F)(F)(F)F.[Ir]. Product ID: ACM870077944. Alfa Chemistry ISO 9001:2015 Certified. | |
| ((4R,5R)-(+)-O-[1-Benzyl-1-(5-methyl-2-phenyl-4,5-dihydrooxazol-4-yl)-2-phenylethyl] (dicyclohexylphosphinite)(1,5-COD)iridium(I) tetrakis(3,5-bis(trifluoromethyl)phenylborate, min. 97% (R,R)-[COD]Ir[cy2PThrePHOX] | ((4R,5R)-(+)-O-[1-Benzyl-1-(5-methyl-2-phenyl-4,5-dihydrooxazol-4-yl)-2-phenylethyl] (dicyclohexylphosphinite)(1,5-COD)iridium(I) tetrakis(3,5-bis(trifluoromethyl)phenylborate, min. 97% (R,R)-[COD]Ir[cy2PThrePHOX]. Uses: New class of hydrogenation catalyst which can convert unfunctionalized styrenyl olefins into alkanes with excellent enantioselectivity. Additional or Alternative Names: 880262-14-6;[((4S,5S)-Cy2-Ubaphox)Ir(COD)]BARF;[((4R,5R)-Cy2-Ubaphox)Ir(COD)]BARF;583844-38-6;MFCD09839141;(R,R)-[COD]Ir[cy2PThrePHOX], 97%,;1,5-Cyclooctadiene{[dibenzyl((4R,5R)-5-methyl-2-phenyl-4,5-dihydro-4-oxazolyl)methyl]dicyclohexylphosphinite |EN:|EP}iridium(I) tetrakis(3,5-bis(trifluoromethyl)phenyl)borate;1,5-Cyclooctadiene{[dibenzyl((4R,5R)-5-methyl-2-phenyl-4,5-dihydro-4-oxazolyl)methyl. Product Category: Iridium series of catalysts. CAS No. 880262-14-6. Molecular formula: C77H70BF24IrNO2P-. Mole weight: 1731.374g/mol. IUPACName: (1Z,5Z)-cycloocta-1,5-diene;dicyclohexyl-[2-[(4R,5R)-5-methyl-2-phenyl-4,5-dihydro-1,3-oxazol-4-yl]-1,3-diphenylpropan-2-yl]oxyphosphane;iridium;tetrakis[3,5-bis(trifluoromethyl)phenyl]boranuide. Canonical SMILES: [B-](C1=CC(=CC(=C1)C(F)(F)F)C(F)(F)F)(C2=CC(=CC(=C2)C(F)(F)F)C(F)(F)F)(C3=CC(=CC(=C3)C(F)(F)F)C( | |
| ((4R,5R)-(+)-O-[1-Benzyl-1-(5-methyl-2-phenyl-4,5-dihydrooxazol-4-yl)-2-phenylethyl] (diphenylphosphinite)(1,5-COD)iridium(I) tetrakis(3,5-bis(trifluoromethyl)phenylborate, min. 97% (R,R)-[COD]Ir[Ph2PThrePHOX] | ((4R,5R)-(+)-O-[1-Benzyl-1-(5-methyl-2-phenyl-4,5-dihydrooxazol-4-yl)-2-phenylethyl] (diphenylphosphinite)(1,5-COD)iridium(I) tetrakis(3,5-bis(trifluoromethyl)phenylborate, min. 97% (R,R)-[COD]Ir[Ph2PThrePHOX]. Uses: New class of hydrogenation catalyst which can convert unfunctionalized styrenyl olefins into alkanes with excellent enantioselectivity. Additional or Alternative Names: 1,5-Cyclooctadiene{[dibenzyl((4R,5R)-5-methyl-2-phenyl-4,5-dihydro-4-oxazolyl)methyl]diphenylphosphinite |EN:|EP}iridium(I) tetrakis(3,5-bis(trifluoromethyl)phenyl)borate; 1,5-Cyclooctadiene{[dibenzyl((4S,5S)-5-methyl-2-phenyl-4,5-dihydro-4-oxazolyl)methyl]diphenylphosphinite |EN:|EP}iridium(I) tetrakis(3,5-bis(trifluoromethyl)phenyl)borate; [((4S,5S)-Ph2-Ubaphox)Ir(COD)]BARF; (4R,5R)-(+)-O-[1-BEN. Product Category: Iridium series of catalysts. CAS No. 880262-16-8. Molecular formula: C77H58BF24IrNO2P-. Mole weight: 1719.278g/mol. IUPACName: (1Z,5Z)-cycloocta-1,5-diene;iridium;[2-[(4R,5R)-5-methyl-2-phenyl-4,5-dihydro-1,3-oxazol-4-yl]-1,3-diphenylpropan-2-yl]oxy-diphenylphosphane;tetrakis[3,5-bis(trifluoromethyl)phenyl]boranuide. Canonical SMILES: [B-](C1=CC(=CC(=C1)C(F)(F)F)C(F)(F)F)(C2=CC(=CC(=C2)C(F)(F)F)C(F)(F)F)(C3=CC(=CC(=C3)C(F)(F)F)C(F)(F)F)C4=CC | |
| ((4S,5S)-(-)-O-[1-Benzyl-1-(5-methyl-2-phenyl-4,5-dihydrooxazol-4-yl)-2-phenylethyl]-dicyclohexylphosphinite)(1,5-COD)iridium(I) tetrakis(3,5-bis(trifluoromethyl)phenylborate, min. 97% (S,S)-[COD]Ir[cy2PThrePHOX] | ((4S,5S)-(-)-O-[1-Benzyl-1-(5-methyl-2-phenyl-4,5-dihydrooxazol-4-yl)-2-phenylethyl]-dicyclohexylphosphinite)(1,5-COD)iridium(I) tetrakis(3,5-bis(trifluoromethyl)phenylborate, min. 97% (S,S)-[COD]Ir[cy2PThrePHOX]. Uses: Iridium-catalyzed asymmetric hydrogenation of n-protected indoles. iridium-catalyzed asymmetric hydrogenation of unfunctionalized enamines. Additional or Alternative Names: (S,S)-[COD]IR[CY2PTHREPHOX]; 583844-38-6; ((4S,5S)-(-)-O-[1-BENZYL-1-(5-METHYL-2-PHENYL-4,5-DIHYDROOXAZOL-4-YL)-2-PHENYLETHYL]-DICYCLOHEXYLPHOSPHINITE)(1,5-COD)IRIDIUM(I) TETRAKIS(3,5-BIS(TRIFLUOROMETHYL)PHENYLBORATE); 1,5-CYCLOOCTADIENE[[DIBENZYL((4S,5S)-5-METHYL-2-PHENYL-4,5-DIHYDRO-4-OXAZOLYL)METHYL]DICYCLOHEXYLPHOSPHINITE KAPPAN:KAPPAP]IRIDIUM(I) TETRAKIS(3,5-BIS(TRIFLUOROMETHYL)PHENYL)BORATE; [((4S,5S)-Cy2-Ubaphox)Ir(COD)]BARF. Product Category: Iridium series of catalysts. CAS No. 583844-38-6. Molecular formula: C77H70BF24IrNO2P-. Mole weight: 1731.374g/mol. IUPACName: cyclooctane;dicyclohexyl-[2-[(4S,5S)-5-methyl-2-phenyl-4,5-dihydro-1,3-oxazol-4-yl]-1,3-diphenylpropan-2-yl]oxyphosphane;iridium;tetrakis[3,5-bis(trifluoromethyl)phenyl]boranuide. Canonical SMILES: [B-](C1=CC(=CC(=C1)C(F)(F)F)C(F)(F)F)(C2=CC(=CC(=C2)C(F)(F)F)C(F)(F)F)(C3=C | |
| 5,5',6,6'-Tetramethyl-3,3'-di-tert-butyl-1,1'-biphenyl-2,2'-diol | 5,5',6,6'-Tetramethyl-3,3'-di-tert-butyl-1,1'-biphenyl-2,2'-diol. Uses: Used as a ligand backbone for metathesis catalysts. 2. used as a ligand backbone in catalytic asymmetric hydrogenation. 3. used as a ligand backbone for asymmetric hydroformylation of allyl cyanide. 4. used as a ligand backbone for phosphoramidite ligands in the asymmetric rh-catalyzed [2+2+2] cycloaddition. 5. used as a ligand backbone for the ring-opening polymerization of cyclic esters. Additional or Alternative Names: BIPHEN-H2; FT-0767390; (S)-(-)-3,3'-Di-tert-butyl-5,5',6,6'-tetramethylbiphenyl-2,2'-diol; (S)-(-)-5,5 inverted exclamation marka,6,6 inverted exclamation marka-Tetramethyl-3,3 inverted exclamation marka-di-tert-butyl-1,1 inverted exclamation marka-biphenyl-2,2 inverted exclamation marka-diol; 5,5',6,6'-Tetramethyl-3,3'-di-tert-butyl-1,1'-biphenyl-2,2'-diol, 97%; (R)-(+)-5,5',6,6'-TETRAMETHYL-3,3'-DI-T-BUTYL-1,1'- BIPHENYL-2,2'-DIOL, 99% (R)-BIPHEN H2; FT-0710826; (S)-()-5,5,6,6-Tetramethyl-3,3-di-tert-butyl-1,1-biphenyl-2,2-diol; AKOS015910403; Acm³29735684. Product Category: Heterocyclic Organic Compound. CAS No. 101203-31-0. Molecular formula: C24H34O2. Mole weight: 354.534g/mol. IUPACName: 6-tert-butyl-2-(3-tert-butyl-2-hydroxy-5,6-dimethylphenyl)-3,4-dimethylphenol. Canonical SMILES: CC1=CC(=C(C(=C1C)C2=C(C(=CC(=C2O)C(C)(C)C)C)C)O)C(C)(C)C. Product ID: ACM101203310. Alfa Chemistry | |
| 9-Ethylcarbazole | 9-Ethylcarbazole (N-Ethylcarbazole) serves as a hydrogen storage material. The introduction of nitrogen (N) into 9-ethylcarbazole can reduce the endothermic nature of the reaction and decrease the dehydrogenation temperature, thereby facilitating the process of hydrogen storage and release [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: N-Ethylcarbazole. CAS No. 86-28-2. Pack Sizes: 25 g; 50 g; 100 g. Product ID: HY-W015003. | |
| Acetyl-3-(2-naphthyl)-D-alanine | Acetyl-3-(2-naphthyl)-D-alanine was used to study the aromatic binding site of α-chymotrypsin. It was used to design an asymmetric synthesis of a new cylindrically chiral and air-stable ferrocenyldiphosphine and its application to rhodium-catalyzed asymmetric hydrogenation. Synonyms: Ac-D-Ala(2-naphthyl)-OH; (R)-N-Acetyl-2-naphthylalanine; Ac-D-2-Nal-OH; (R)-2-ACETAMIDO-3-(NAPHTHALEN-2-YL)PROPANOIC ACID; N-Acetyl-3-(2-naphthyl)-D-alanine; 2-Naphthalenepropanoic acid, a-(acetylamino)-, (aR)-; Ac-D-Ala(2-Naph)-OH. Grade: ≥ 98% (HPLC). CAS No. 37440-01-0. Molecular formula: C15H15NO3. Mole weight: 257.28. | |
| AD-mix-α | AD-mix-α is a mixture of organic compounds, commonly used to distinguish and identify asymmetric carbon atoms in chiral compounds. It consists of compounds containing catalytically active metals and chiral ligands. AD-mix-α is widely used in various organic synthesis reactions, such as hydrogenation, addition, and carbonylation reactions, to increase yield and reduce the formation of side reaction products. Although it has no direct application in the medical field, it plays an important role in the pharmaceutical industry and chemical research. Uses: Scientific research. Group: Biochemical assay reagents. CAS No. 153130-59-7. Pack Sizes: 1 g; 5 g. Product ID: HY-24312. | |
| Androstenediol 17-Acetate | Androstenediol 17-Acetate is used in synthetic preparation for direct organocatalytic stereoselective transfer hydrogenation of conjugated olefins of steroids. Androstenediol 17-Acetate is also obtained from Dehydro Epiandrosterone (D229585) which is a major secretory steroidal product of the adrenal gland; secretion progresively declines with aging. May have estrogen-or androgen-like effects depending on the hormonal milieu. Intracellularly converted to androstenedione. It is used in treatment of menopausal syndrome. Group: Biochemicals. Grades: Highly Purified. CAS No. 5937-72-4. Pack Sizes: 1mg, 5mg. Molecular Formula: C21H32O3, Molecular Weight: 332.48. US Biological Life Sciences. | Worldwide |
| Antiblastin | Antiblastin is an antifungal antibiotic produced by Monilia antipiriculariae. Catalytic hydrogenation to generate tridecane. Synonyms: Mycomycin; UNII-398491Y0IE. CAS No. 544-51-4. Molecular formula: C13H10O2. Mole weight: 198.22. | |
| Avermectin A1a | Avermectin A1a is produced by the strain of Streptomyces avermitilis. It stimulates nerve cells to release Y-aminobutyric acid (GABA), which blocks the transmission of signals from the central nervous system to the motor nerve. It is not resistant to bacteria and fungi, but has strong activity to nematode parasites such as ancylostoma and Pteria, as well as insects such as flies. Abamectin B1a has the highest activity. Ivermectin obtained by catalytic hydrogenation contains 22 23- dihydroabamectin B1a (above 80%) and 22 23 dioxabamectin B1b (below 20%). Less active than B1a but less toxic. Used as repellent (subcutaneous or oral) for cattle, sheep and pigs, it is also effective against human filariasis. Synonyms: SCHEMBL1681257. CAS No. 65195-51-9. Molecular formula: C49H74O14. Mole weight: 887.10. | |
| Avermectin A2a | Avermectin A2a is produced by the strain of Streptomyces avermitilis. It stimulates nerve cells to release Y-aminobutyric acid (GABA), which blocks the transmission of signals from the central nervous system to the motor nerve. It is not resistant to bacteria and fungi, but has strong activity to nematode parasites such as ancylostoma and Pteria, as well as insects such as flies. Abamectin B1a had the highest activity. Ivermectin obtained by catalytic hydrogenation contains 22,23-dihydroabamectin B1a (above 80%) and 22,23 dioxabamectin B1b(below 20%). Less active than B1a but less toxic. Used as repellent (subcutaneous or oral) for cattle, sheep and pigs, it is also effective against human filariasis. Synonyms: Avermectin A1a; SCHEMBL1681224. CAS No. 50914-15-3. Molecular formula: C49H76O15. Mole weight: 905.12. | |
| Avermectin B2a | Avermectin B2a is produced by the strain of Streptomyces avermitilis. It stimulates nerve cells to release Y-aminobutyric acid (GABA), which blocks the transmission of signals from the central nervous system to the motor nerve. It is not resistant to bacteria and fungi, but has strong activity to nematode parasites such as ancylostoma and Pteria, as well as insects such as flies. Abamectin B1a has the highest activity. Ivermectin obtained by catalytic hydrogenation contains 22 23- dihydroabamectin B1a (above 80%) and 22 23 dioxabamectin B1b (below 20%). Less active than B1a but less toxic. Used as repellent (subcutaneous or oral) for cattle, sheep and pigs, it is also effective against human filariasis. Synonyms: Ivermectin EP Impurity C; (23S)-5-O-demethyl-23-hydroxy-22,23-dihydro-avermectin A1a. CAS No. 65195-57-5. Molecular formula: C48H74O15. Mole weight: 891.09. | |
| Benzeneruthenium(II) Chloride Dimer | Benzeneruthenium(II) Chloride Dimer is a catalyst for SNAr reactions of fluoroarenes and cyclic amines, a precatalyst for the hydrogenation of β-keto esters and a precursor for the preparation of other ruthenium catalysts. Group: Biochemicals. Alternative Names: Bis ( η 6- Benzene ) di- μ -chloro dichloro diruthenium ; (Benzene) dichlororuthenium DimerBenzeneruthenium Dichloride Dimer; Bis((η6-benzene)chloro(μ-chloro)ruthenium); Bis ( (η 6-benzene) dichlororuthenium) ; Bis ( Benzene ) di- μ -chloro dichloro diruthenium ; Bis ( Benzene ) tetrachlorodiruthenium ; Bis ( η 6- Benzene ) tetrachlorodiruthenium ; Bis(?-benzeneruthenium dichloride); Bis[ (benzene) dichlororuthenium]; Bis[dichloro[η6-(benzene)]ruthenium]; Di Benzene tetrachlorodiruthenium ; μ -Dichloro-bis ( Benzene chlororuthenium (II) ) . Grades: Highly Purified. CAS No. 37366-09-9. Pack Sizes: 1g, 5g. Molecular Formula: C12H12Cl4Ru2, Molecular Weight: 500.18. US Biological Life Sciences. | Worldwide |
| Bis(1,5-cyclooctadiene)rhodium(I) tetrafluoroborate | Bis(1,5-cyclooctadiene)rhodium(I) tetrafluoroborate. Uses: Asymmetric reactions; c-h activation; hydroformylation; hydrogenation→asymmetric hydrogenation; hydrosilylation; isomerization. Additional or Alternative Names: Bis(cycloocta-1,5-diene)rhodium(I) tetrafluoroborate. Product Category: Rhodium series of catalysts. Appearance: Orange red crystalline powder. CAS No. 35138-22-8. Molecular formula: C16H24BF4Rh. Mole weight: 406.07. Purity: 0.99. IUPACName: (1Z,5Z)-cycloocta-1,5-diene;rhodium;tetrafluoroborate. Canonical SMILES: [B-](F)(F)(F)F.C1CC=CCCC=C1.C1CC=CCCC=C1.[Rh]. ECNumber: 460-220-1. Product ID: ACM35138228-2. Alfa Chemistry ISO 9001:2015 Certified. | |
| Bis(1,5-cyclooctadiene)rhodium(I) trifluoromethanesulfonate | Bis(1,5-cyclooctadiene)rhodium(I) trifluoromethanesulfonate. Uses: Asymmetric reactions; c-h activation; hydroformylation; hydrogenation→asymmetric hydrogenation. Additional or Alternative Names: (1Z,5Z)-cycloocta-1,5-diene;rhodium;trifluoromethanesulfonate. Product Category: Rhodium series of catalysts. Appearance: Red brown powder. CAS No. 99326-34-8. Molecular formula: C17H24F3O3RhS. Mole weight: 468.34. Purity: 0.99. IUPACName: (1Z,5Z)-cycloocta-1,5-diene;rhodium;trifluoromethanesulfonate. Canonical SMILES: C1CC=CCCC=C1.C1CC=CCCC=C1.C(F)(F)(F)S(=O)(=O)[O-].[Rh]. Product ID: ACM99326348-2. Alfa Chemistry ISO 9001:2015 Certified. | |
| Butylene Glycol | Butylene glycol occurs as a clear, colorless, viscous liquid with a sweet flavor and bitter aftertaste. Synonyms: Butane-1,3-diol; 1,3-butylene glycol; b-butylene glycol; 1,3-dihy- droxybutane; methyltrimethylene glycol. CAS No. 107-88-0. Product ID: PE0400. Molecular formula: C4H10O2. Mole weight: 90.14. Category: Preservatives; Humectants; Solvents. Product Keywords: Pharmaceutical Excipients; Other Materials; Humectants; Butylene Glycol; PE0400; 3XUS85K0RA; 107-88-0; 107-88-0. UNII: 3XUS85K0RA. Chemical Name: 1,3-Butanediol. Grade: Pharmceutical Excipients. Dosage Form: Transdermal patches;topical gel patches/medicated plasters. Stability and Storage Conditions: Butylene glycol is hygroscopic and should be stored in a well-closed container in a cool, dry, well-ventilated place. When heated to decomposition, butylene glycol emits acrid smoke and irritating fumes. Source and Preparation: Butylene glycol is prepared by catalytic hydrogenation of aldol using Raney nickel. Applications: Butylene glycol is used as a solvent and cosolvent for injectables.It is used in topical ointments, creams, and lotions,and it is also used as a vehicle in transdermal patches. Butylene glycol is a good solvent for many pharmaceuticals, especially estrogenic substances.In an oil-in-water emulsion, butylene glycol exerts its best antimicrobial effects at 8% concentration.Higher concentrations above 16.7% are required to inhibit fungal |  |
| Carbonylchlorobis(triphenylphosphine)iridium(I) | Carbonylchlorobis(triphenylphosphine)iridium(I). Uses: Catalyst for the intramolecular carbonylative [2+2+1] cycloaddition of allenynes. catalyst for the selective hydrogenation of myrcene. catalyst for silylation of ortho-functionalized aryl halides with hydrosilanes. catalyst for synthesis of aldenamines from carboxamides by silane-reduction/dehydration under mild conditions. hydrogen atom transfer catalyst for radical cyclizations. complex for photocatalytic alkane dehydrogenation. catalyst for chemoselective reductive nucleophilic addition to n-methoxyamides. catalyst for chemoselective reductive alkynylation of tertiary amides. Additional or Alternative Names: Bis(triphenylphosphine)iridium(I) carbonyl chloride. Product Category: Iridium series of catalysts. Appearance: Crystal. CAS No. 14871-41-1. Molecular formula: C37H32ClIrOP2. Mole weight: 782.3. Purity: 0.99. IUPACName: formaldehyde;iridium;triphenylphosphane;chloride. Canonical SMILES: C=O.C1=CC=C(C=C1)P(C2=CC=CC=C2)C3=CC=CC=C3.C1=CC=C(C=C1)P(C2=CC=CC=C2)C3=CC=CC=C3.[Cl-].[Ir]. ECNumber: 238-941-6. Product ID: ACM14871411-1. Alfa Chemistry ISO 9001:2015 Certified. Categories: Carbonylbis(triphenylphosphine)iridium(I) Chloride. | |
| Carbonylchlorohydridotris(triphenylphosphine)ruthenium(II) | Carbonylchlorohydridotris(triphenylphosphine)ruthenium(II). Uses: Hydroformylation; hydrogenation→transfer hydrogenation; isomerization. Additional or Alternative Names: Carbonylchlorohydridotris(triphenylphosphine)ruthenium(II);16971-33-8;MFCD00049804;Ru(CO)ClH[P(C6H5)3]3;[(C6H5)3P]3Ru(CO)(Cl)H;AKOS024258164. Product Category: Ruthenium series catalysts. Appearance: beige. CAS No. 16971-33-8. Molecular formula: C55H46ClOP3Ru. Mole weight: 952.41. Purity: Metal purity 99.95. IUPACName: chloro(hydrido)ruthenium;formaldehyde;triphenylphosphane. Canonical SMILES: C=O.C1=CC=C(C=C1)P(C2=CC=CC=C2)C3=CC=CC=C3.C1=CC=C(C=C1)P(C2=CC=CC=C2)C3=CC=CC=C3.C1=CC=C(C=C1)P(C2=CC=CC=C2)C3=CC=CC=C3.Cl[RuH]. ECNumber: 241-051-0. Product ID: ACM16971338-1. Alfa Chemistry ISO 9001:2015 Certified. Categories: Carbonylchlorohydrotris(triphenylphosphine)ruthenium. | |
| Carbonyl(dihydrido)tris(triphenylphosphine)ruthenium(II) | Carbonyl(dihydrido)tris(triphenylphosphine)ruthenium(II). Uses: Catalyst for the arylation (or alkenylation) of anthraquinone and pbi. catalytic c-c bond formation. transfer hydrogenative coupling of isoprene to alcohols or aldehydes. alkanes (and alkenes) from alcohols by tandem hydrogen transfer and condensation. catalyst for the conversion of primary alcohols and aldehydes into methyl esters. precatalyst for hydrogen production by means of alcohol dehydrogenation. Additional or Alternative Names: 25360-32-1;Carbonyl(dihydrido)tris(triphenylphosphine)ruthenium(II);Carbonyldihydridotris(triphenylphosphine)ruthenium(II);Dihydridocarbonyltris(triphenylphosphine)ruthenium;C55H47OP3Ru;[(C6H5)3P]3Ru(CO)H2;AKOS024258165;Carbonyl(dihydrido)tris(triphenylphosphine)ruthenium (II). Product Category: Ruthenium series catalysts. CAS No. 25360-32-1. Molecular formula: C55H49OP3Ru. Mole weight: 919.987g/mol. IUPACName: formaldehyde;ruthenium dihydride;triphenylphosphane. Canonical SMILES: C=O.C1=CC=C(C=C1)P(C2=CC=CC=C2)C3=CC=CC=C3.C1=CC=C(C=C1)P(C2=CC=CC=C2)C3=CC=CC=C3.C1=CC=C(C=C1)P(C2=CC=CC=C2)C3=CC=CC=C3.[RuH2]. Product ID: ACM25360321. Alfa Chemistry ISO 9001:2015 Certified. | |
| Carbonylhydrido[6-(di-t-butylphosphinomethylene)-2-(N,N-diethylaminomethyl)-1,6-dihydropyridine]ruthenium(II), min. 98% Milstein Catalyst | Carbonylhydrido[6-(di-t-butylphosphinomethylene)-2-(N,N-diethylaminomethyl)-1,6-dihydropyridine]ruthenium(II), min. 98% Milstein Catalyst. Uses: Ruthenium catalyst for the direct synthesis of amides from alcohols and primary amines. ruthenium catalyst for the hydrogenation of esters in high yields under mild pressure and neutral conditions. ruthenium catalyst for the dehydrogenative coupling of alcohols to form esters in high yields under neutral conditions. ruthenium catalyst for the synthesis of amides from esters and amines with liberation of hydrogen gas. ruthenium catalyst for the hydrogenation of 3-methyl-2-oxalidinone. Additional or Alternative Names: 863971-63-5;Carbonylhydrido[6-(di-t-butylphosphinomethylene)-2-(N,N-diethylaminomethyl)-1,6-dihydropyridine]ruthenium(II);DTXSID40856225;Ruthenium(2+) hydride (2E)-2-[(di-tert-butylphosphanyl)methylidene]-6-[(diethylamino)methyl]-2H-pyridin-1-ide--carbon monooxide (1/1/1/1). Product Category: Ruthenium series catalysts. CAS No. 863971-63-5. Molecular formula: C20H35N2OPRu. Mole weight: 451.557g/mol. IUPACName: carbon monoxide;N-[[(6E)-6-(ditert-butylphosphanylmethylidene)pyridin-1-id-2-yl]methyl]-N-ethylethanamine;hydride;ruthenium(2+). Canonical SMILES: [H-].CCN(CC)CC1=CC=CC(=CP(C(C)(C)C)C(C)(C)C)[N-]1.[C-]#[O+].[Ru+2]. Product ID: ACM863971635. A | |
| Carbonylhydridotris(triphenylphosphine)iridium(I) | Carbonylhydridotris(triphenylphosphine)iridium(I). Uses: Catalyst for ring-opening isomerization of unsymmetrically substituted methylenecyclopropanes into 1,3-dienes catalyst for asymmetric transfer hydrogenation of aromatic ketones under base-free conditions catalyst for c-f bond activation for the c-s cross-coupling of aryl fluorides with diaryl disulfides to synthesize thioethers. Additional or Alternative Names: Carbon monoxide;iridium;triphenylphosphane. Product Category: Iridium series of catalysts. Appearance: Powder. CAS No. 17250-25-8. Molecular formula: C55H45IrOP3. Mole weight: 1007.1. Purity: 0.99. IUPACName: carbon monoxide;iridium;triphenylphosphane. Canonical SMILES: [C-]#[O+].C1=CC=C(C=C1)P(C2=CC=CC=C2)C3=CC=CC=C3.C1=CC=C(C=C1)P(C2=CC=CC=C2)C3=CC=CC=C3.C1=CC=C(C=C1)P(C2=CC=CC=C2)C3=CC=CC=C3.[Ir]. ECNumber: 241-282-7. Product ID: ACM17250258-1. Alfa Chemistry ISO 9001:2015 Certified. | |
| Chloro(1,5-cyclooctadiene)iridium(I) dimer | Chloro(1,5-cyclooctadiene)iridium(I) dimer. Uses: 1. precursor to catalysts for the asymmetric hydrogenation of tri- and tetrasubstituted olefins. 2. precursor to catalyst for enantioselective reduction of imines. 3. precursor to catalyst for allylic alkylation. 4. precursor to catalyst for allylic amination and etherification. 5. precursor to catalyst for the reaction of aroyl chlorides with internal alkynes to produce substituted naphthalenes and anthracenes. 6. ir-catalyzed addition of acid chlorides to terminal alkynes. 7. intramolecular hydroamination of unactivated alkenes with secondary alkyl- and arylamines. 8. enantioselective [2+2] cycloaddition. 9. silyl-directed, ir-catalyzed ortho-borylation of arenes. 10. ir-catalyzed cross-coupling of styrene derivatives with allylic carbonates. 11. transfer hydrogenative c-c coupling. Additional or Alternative Names: Bis(1,5-cyclooctadiene)diiridium(I) dichloride. Product Category: Iridium series of catalysts. Appearance: Red brown powder. CAS No. 12112-67-3. Molecular formula: C16H24Cl2Ir2. Mole weight: 671.71. Purity: 0.99. IUPACName: (1Z,5Z)-cycloocta-1,5-diene;iridium;dichloride. Canonical SMILES: C1CC=CCCC=C1.C1CC=CCCC=C1.[Cl-].[Cl-].[Ir].[Ir]. ECNumber: 235-170-7. Product ID: ACM12112673-4. Alfa Chemistry ISO 9001:2015 Certified. | |
| Chloro(1,5-cyclooctadiene)rhodium(I) dimer | Chloro(1,5-cyclooctadiene)rhodium(I) dimer. Uses: Catalyst for coupling 1,3-dienes with activate methylene compounds. rhodium source for various asymmetric hydrogenation systems and asymmetric hydrosilylation of ketones. rhodium source for asymmetric reductive aldol reaction. cis-hydroboration of terminal alkynes. rhodium source for [5 + 2] additions. highly enantioselective for [2+2+2] carbocyclization reactions. enantioselective hydroboration of cyclopropenes. Group: Salt. Alternative Names: Bis(cycloocta-1,5-diene)dichlorodirhodium. CAS No. 12092-47-6. Product ID: (1Z,5Z)-cycloocta-1,5-diene; rhodium; dichloride. Molecular formula: 493.08. Mole weight: C16H24Cl2Rh2. C1CC=CCCC=C1. C1CC=CCCC=C1. [Cl-]. [Cl-]. [Rh]. [Rh]. InChI=1S/2C8H12. 2ClH. 2Rh/c2*1-2-4-6-8-7-5-3-1; /h2*1-2, 7-8H, 3-6H2; 2*1H; /p-2/b2*2-1-, 8-7-. PDJQCHVMABBNQW-MIXQCLKLSA-L. 98%. | |
| Chlorodihydrido[bis(2-di-i-propylphosphinoethyl)amine]iridium(III), min. 98% | Chlorodihydrido[bis(2-di-i-propylphosphinoethyl)amine]iridium(III), min. 98%. Uses: Amination of aliphatic alcohols and diols using an iridium pincer catalyst. iridium-catalyzed hydrogenation of carboxylic acid esters. Additional or Alternative Names: Chlorodihydrido[bis(2-di-i-propylphosphinoethyl)amine]iridium(III);791629-96-4;SCHEMBL1465922;AKOS024259169;Chlorodihydrido[bis(2-diisopropylphosphino)ethylamine]iridium(III), mixture of isomers, 97%;chloro(dihydrido)iridium;2-di(propan-2-yl)phosphanyl-N-[2-di(propan-2-yl)phosphanylethyl]ethanamine. Product Category: Iridium series of catalysts. CAS No. 791629-96-4. Molecular formula: C16H39ClIrNP2. Mole weight: 535.11g/mol. IUPACName: chloro(dihydrido)iridium;2-di(propan-2-yl)phosphanyl-N-[2-di(propan-2-yl)phosphanylethyl]ethanamine. Canonical SMILES: CC(C)P(CCNCCP(C(C)C)C(C)C)C(C)C.Cl[IrH2]. Product ID: ACM791629964. Alfa Chemistry ISO 9001:2015 Certified. | |
| Chloro[(R)-(+)-2,2'-bis(diphenylphosphino)-5,5',6,6',7,7',8,8'-octahydro-1,1'-binaphthyl](p-cymene)ruthenium(II) chloride [RuCl(p-cymene)((R)-H8-binap)]Cl | Chloro[(R)-(+)-2,2'-bis(diphenylphosphino)-5,5',6,6',7,7',8,8'-octahydro-1,1'-binaphthyl](p-cymene)ruthenium(II) chloride [RuCl(p-cymene)((R)-H8-binap)]Cl. Uses: Biaryl bisphosphine ligand. the h8-binap ligand, as the ruthenium complex, catalyzes hydrogenation of unsaturated carboxylic acids to a higher ee than does binap. the ruthenium catalyzed hydrogenation of aryl propenoic acid to produce the drug ibuprofen. Additional or Alternative Names: (R)-RUCL[P-CYMENE(H8-BINAP)]CL; [RUCL(P-CYMENE)((S)-H8-BINAP)]CL; SC10137; MFCD09753016; CHLORO[(R)-(+)-2,2'-BIS(DIPHENYLPHOSPHINO)-5,5',6,6',7,7',8,8'-OCTAHYDRO-1,1'-BINAPHTHYL](P-CYMENE)RUTHENIUM(II) CHLORIDE; [RUCL(P-CYMENE)((R)-H8-BINAP)]CL. Product Category: Ruthenium series catalysts. CAS No. 944451-26-7. Molecular formula: C54H54Cl2P2Ru. Mole weight: 936.944g/mol. IUPACName: dichlororuthenium;[1-(2-diphenylphosphanyl-5,6,7,8-tetrahydronaphthalen-1-yl)-5,6,7,8-tetrahydronaphthalen-2-yl]-diphenylphosphane;1-methyl-4-propan-2-ylbenzene. Canonical SMILES: CC1=CC=C(C=C1)C(C)C.C1CCC2=C(C1)C=CC(=C2C3=C(C=CC4=C3CCCC4)P(C5=CC=CC=C5)C6=CC=CC=C6)P(C7=CC=CC=C7)C8=CC=CC=C8.Cl[Ru]Cl. Product ID: ACM944451267. Alfa Chemistry ISO 9001:2015 Certified. | |
| cis-2-Butene-1,4-diol | cis-2-Butene-1,4-diol, an industrial product, can be used for the synthesis of antiviral product oxetanocin A. cis-2-Butene-1,4-diol is a probe for studying isomerization versus hydrogenation and hydrogenolysis reactions [1] [2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 6117-80-2. Pack Sizes: 10 mM * 1 mL; 500 mg; 1 g. Product ID: HY-W027631. | |
| Diacetato{(R)-(+)-2,2'-bis[di(3,5-xylyl)phosphino]-1,1'-binaphthyl}ruthenium(II) Ru(OAc)2[(R)-xylbinap] | Diacetato{(R)-(+)-2,2'-bis[di(3,5-xylyl)phosphino]-1,1'-binaphthyl}ruthenium(II) Ru(OAc)2[(R)-xylbinap]. Uses: Catalyst system used for asymmetric hydrogenation. Additional or Alternative Names: DIACETATO[(S)-(-)-2,2'-BIS[DI(3,5-XYLYL)PHOSPHINO]-1,1'-BINAPHTHYL]RUTHENIUM(II); RU(OAC)2[(S)-XYLBINAP]; 374067-50-2; Diacetoxyruthenium; RU(OAC)2[(R)-XYLBINAP]; (R)-Ru(OAc)2(DM-BINAP); DIACETATO[(R)-(+)-2,2'-BIS[DI(3,5-XYLYL)PHOSPHINO]-1,1'-BINAPHTHYL]RUTHENIUM(II); Ru[(S)-DM-BINAP](OCOCH3)2; 374067-49-9; MFCD09753022. Product Category: Ruthenium series catalysts. CAS No. 374067-50-2. Molecular formula: C56H56O4P2Ru. Mole weight: 956.078g/mol. IUPACName: acetic acid;[1-[2-bis(3,5-dimethylphenyl)phosphanylnaphthalen-1-yl]naphthalen-2-yl]-bis(3,5-dimethylphenyl)phosphane;ruthenium. Canonical SMILES: CC1=CC(=CC(=C1)P(C2=C(C3=CC=CC=C3C=C2)C4=C(C=CC5=CC=CC=C54)P(C6=CC(=CC(=C6)C)C)C7=CC(=CC(=C7)C)C)C8=CC(=CC(=C8)C)C)C.CC(=O)O.CC(=O)O.[Ru]. Product ID: ACM374067502. Alfa Chemistry ISO 9001:2015 Certified. | |
| Diacetato[(R)-(+)-2,2'-bis(diphenylphosphino)-1,1'-binaphthyl]ruthenium(II) Ru(OAc)2[(R)-binap] | Diacetato[(R)-(+)-2,2'-bis(diphenylphosphino)-1,1'-binaphthyl]ruthenium(II) Ru(OAc)2[(R)-binap]. Uses: Catalyst system that exhibits very high catalytic activity and enantioselectivity in the hydrogenation of a wide range of substrates. catalyst used in the synthesis of β-amino acids by hydrogenation. Additional or Alternative Names: Bis(acetato)(binap) ruthenium; Diacetato[(R)-(+)-2,2 inverted exclamation marka-bis(diphenylphosphino)-1,1 inverted exclamation marka-binaphthyl]ruthenium(II); Diacetato[(R)-(+)-2,2'-bis(diphenylphosphino)-1,1'-binaphthyl]ruthenium(II), Ru(OAc)2[(R)-binap]; DIACETATO[(R)-(+)-2,2'-BIS(DIPHENYLPHOSPHINO)-1,1'-BINAPHTHYL]RUTHENIUM(II); RU(OAC)2[(R)-BINAP]; DIACETATO[(S)-(-)-2,2'-BIS(DIPHENYLPHOSPHINO)-1,1'-BINAPHTHYL]RUTHENIUM(II); Diacetato[(S)-(-)-2,2 inverted exclamation marka-bis(diphenylphosphino)-1,1 inverted exclamation marka-binaphthyl]ruthenium(II); SC10141; 325146-81-4. Product Category: Ruthenium series catalysts. CAS No. 325146-81-4. Molecular formula: C48H40O4P2Ru. Mole weight: 843.862g/mol. IUPACName: acetic acid;[1-(2-diphenylphosphanylnaphthalen-1-yl)naphthalen-2-yl]-diphenylphosphane;ruthenium. Canonical SMILES: CC(=O)O.CC(=O)O.C1=CC=C(C=C1)P(C2=CC=CC=C2)C3=C(C4=CC=CC=C4C=C3)C5=C(C=CC6=CC=CC=C65)P(C7=CC=CC=C7)C8=CC=CC=C8.[Ru]. Product ID: ACM325146814. Alfa Chemistry ISO 9001:2015 Certified. | |
| Diacetato[(R)-(+)-2,2'-bis(diphenylphosphino)-5,5',6,6',7,7',8,8'-octahydro-1,1'-binaphthyl]ruthenium(II) Ru(OAc)2[(R)-H8-binap] | Diacetato[(R)-(+)-2,2'-bis(diphenylphosphino)-5,5',6,6',7,7',8,8'-octahydro-1,1'-binaphthyl]ruthenium(II) Ru(OAc)2[(R)-H8-binap]. Uses: Biaryl bisphosphine ligand. the h8-binap ligand, as the ruthenium complex, catalyzes hydrogenation of unsaturated carboxylic acids to a higher ee than does binap. the ruthenium catalyzed hydrogenation of aryl propenoic acid to produce the drug ibuprofen. Additional or Alternative Names: DIACETATO[(R)-2,2'-BIS(DIPHENYLPHOSPHINO)-5,5',6,6',7,7',8,8'-OCTAHYDRO-1,1'-BINAPHTHYL]RUTHENIUM(II); RU(OAC)2[(S)-H8-BINAP]; DIACETATO[(S)-(-)-2,2'-BIS(DIPHENYLPHOSPHINO)-5,5',6,6',7,7',8,8'-OCTAHYDRO-1,1'-BINAPHTHYL]RUTHENIUM(II); RU(OAC)2[(R)-H8-BINAP]; 142962-95-6; Diacetato[(S)-(-)-2,2 inverted exclamation marka-bis(diphenylphosphino)-5,5 inverted exclamation marka,6,6 inverted exclamation m. Product Category: Ruthenium series catalysts. CAS No. 374067-51-3. Molecular formula: C48H48O4P2Ru. Mole weight: 851.926g/mol. IUPACName: acetic acid;[1-(2-diphenylphosphanyl-5,6,7,8-tetrahydronaphthalen-1-yl)-5,6,7,8-tetrahydronaphthalen-2-yl]-diphenylphosphane;ruthenium. Canonical SMILES: CC(=O)O.CC(=O)O.C1CCC2=C(C1)C=CC(=C2C3=C(C=CC4=C3CCCC4)P(C5=CC=CC=C5)C6=CC=CC=C6)P(C7=CC=CC=C7)C8=CC=CC=C8.[Ru]. Product ID: ACM374067513. Alfa Chemistry ISO 9001:2015 Certified. | |
| Diacetato[(R)-(+)-2,2'-bis(di-p-tolylphosphino)-1,1'-binaphthyl]ruthenium(II) Ru(OAc)2[(R)-tolbinap] | Diacetato[(R)-(+)-2,2'-bis(di-p-tolylphosphino)-1,1'-binaphthyl]ruthenium(II) Ru(OAc)2[(R)-tolbinap]. Uses: Catalyst system that exhibits high catalytic activity and enantioselectivity in the hydrogenation of enamines. Additional or Alternative Names: RU(OAC)2[(R)-TOLBINAP]; 106681-15-6; Ru[(S)-T-BINAP](OCOCH3)2; Diacetato[(S)-(-)-2,2 inverted exclamation marka-bis(di-p-tolylphosphino)-1,1 inverted exclamation marka-binaphthyl]ruthenium(II); DIACETATO[(R)-(+)-2,2'-BIS(DI-P-TOLYLPHOSPHINO)-1,1'-BINAPHTHYL]RUTHENIUM(II); 116128-29-1; I14-34094; Diacetato[(R)-2,2 inverted exclamation marka-bis(di-p-tolylphosphino)-1,1 inverted exclamation marka-binaphthyl]ruthenium(II); DIACETATO[(R)-2,2'-BIS(DI-P-TOLYLPHOSPHINO)-1,1'-BINAPHTHYL]RUTHENIUM(II). Product Category: Ruthenium series catalysts. CAS No. 116128-29-1. Molecular formula: C52H48O4P2Ru. Mole weight: 899.97g/mol. IUPACName: acetic acid;[1-[2-bis(4-methylphenyl)phosphanylnaphthalen-1-yl]naphthalen-2-yl]-bis(4-methylphenyl)phosphane;ruthenium. Canonical SMILES: CC1=CC=C(C=C1)P(C2=CC=C(C=C2)C)C3=C(C4=CC=CC=C4C=C3)C5=C(C=CC6=CC=CC=C65)P(C7=CC=C(C=C7)C)C8=CC=C(C=C8)C.CC(=O)O.CC(=O)O.[Ru]. Product ID: ACM116128291. Alfa Chemistry ISO 9001:2015 Certified. | |
| Diacetato{(S)-(-)-2,2'-bis[di(3,5-xylyl)phosphino]-1,1'-binaphthyl}ruthenium(II) Ru(OAc)2[(S)-xylbinap] | Diacetato{(S)-(-)-2,2'-bis[di(3,5-xylyl)phosphino]-1,1'-binaphthyl}ruthenium(II) Ru(OAc)2[(S)-xylbinap]. Uses: Catalyst system used for asymmetric hydrogenation. Additional or Alternative Names: C56H54O4P2Ru; Diacetato[(R)-2,2 inverted exclamation marka-bis[di(3,5-xylyl)phosphino]-1,1 inverted exclamation marka-binaphtyl]ruthenium(II); MFCD09753022; 374067-49-9; (S)-Ru(OAc)2(DM-BINAP); Diacetato{(R)-(+)-2,2'-bis[di(3,5-xylyl)phosphino]-1,1'-binaphthyl}ruthenium(II), Ru(OAc)2[(R)-xylbinap]; DIACETATO[(S)-(-)-2,2'-BIS[DI(3,5-XYLYL)PHOSPHINO]-1,1'-BINAPHTHYL]RUTHENIUM(II); 374067-50-2; RU(OAC)2[(R)-XYLBINAP]; RU(OAC)2[(S)-XYLBINAP]. Product Category: Ruthenium series catalysts. CAS No. 374067-49-9. Molecular formula: C56H56O4P2Ru. Mole weight: 956.078g/mol. IUPACName: acetic acid;[1-[2-bis(3,5-dimethylphenyl)phosphanylnaphthalen-1-yl]naphthalen-2-yl]-bis(3,5-dimethylphenyl)phosphane;ruthenium. Canonical SMILES: CC1=CC(=CC(=C1)P(C2=C(C3=CC=CC=C3C=C2)C4=C(C=CC5=CC=CC=C54)P(C6=CC(=CC(=C6)C)C)C7=CC(=CC(=C7)C)C)C8=CC(=CC(=C8)C)C)C.CC(=O)O.CC(=O)O.[Ru]. Product ID: ACM374067499. Alfa Chemistry ISO 9001:2015 Certified. | |
| Diacetato[(S)-(-)-2,2'-bis(diphenylphosphino)-1,1'-binaphthyl]ruthenium(II) Ru(OAc)2[(S)-binap] | Diacetato[(S)-(-)-2,2'-bis(diphenylphosphino)-1,1'-binaphthyl]ruthenium(II) Ru(OAc)2[(S)-binap]. Uses: 1. catalyst system that exhibits very high catalytic activity and enantioselectivity in the hydrogenation of a wide range of substrates. 2. catalyst used in the synthesis of β-amino acids by hydrogenation. Additional or Alternative Names: (S)-Ru(OAc)2(BINAP); RU-BINAP; DIACETATO[(R)-(+)-2,2'-BIS(DIPHENYLPHOSPHINO)-1,1'-BINAPHTHYL]RUTHENIUM(II); 104713-03-3; Diacetato[(S)-(-)-2,2 inverted exclamation marka-bis(diphenylphosphino)-1,1 inverted exclamation marka-binaphthyl]ruthenium(II); 325146-81-4; DIACETATO[(R)-(-)-2,2'-BIS(DIPHENYLPHOSPHINO)-1,1'-BINAPHTHYL]RUTHENIUM(II); 261948-85-0; RU(OAC)2[(R)-BINAP]; DIACETATO[(S)-(-)-2,2'-BIS(DIPHENYLPHOSPHINO)-1,1'-BINAPHTHYL]RUTHENIUM(II). Product Category: Ruthenium series catalysts. CAS No. 261948-85-0. Molecular formula: C48H40O4P2Ru. Mole weight: 843.862g/mol. IUPACName: acetic acid;[1-(2-diphenylphosphanylnaphthalen-1-yl)naphthalen-2-yl]-diphenylphosphane;ruthenium. Canonical SMILES: CC(=O)O.CC(=O)O.C1=CC=C(C=C1)P(C2=CC=CC=C2)C3=C(C4=CC=CC=C4C=C3)C5=C(C=CC6=CC=CC=C65)P(C7=CC=CC=C7)C8=CC=CC=C8.[Ru]. Product ID: ACM261948850. Alfa Chemistry ISO 9001:2015 Certified. | |
| Diacetato[(S)-(-)-2,2'-bis(diphenylphosphino)-5,5',6,6',7,7',8,8'-octahydro-1,1'-binaphthyl]ruthenium(II) Ru(OAc)2[(S)-H8-binap] | Diacetato[(S)-(-)-2,2'-bis(diphenylphosphino)-5,5',6,6',7,7',8,8'-octahydro-1,1'-binaphthyl]ruthenium(II) Ru(OAc)2[(S)-H8-binap]. Uses: Biaryl bisphosphine ligand. the h8-binap ligand, as the ruthenium complex, catalyzes hydrogenation of unsaturated carboxylic acids to a higher ee than does binap. the ruthenium catalyzed hydrogenation of aryl propenoic acid to produce the drug ibuprofen. Additional or Alternative Names: Diacetato[(R)-(+)-2,2'-bis(diphenylphosphino)-5,5',6,6',7,7',8,8'-octahydro-1,1'-binaphthyl]ruthenium(II), Ru(OAc)2[(R)-H8-binap]; Diacetato[(R)-2,2 inverted exclamation marka-bis(diphenylphosphino)-5,5 inverted exclamation marka,6,6 inverted exclamation marka,7,7 inverted exclamation marka,8,8 inverted exclamation marka-octahydro-1,1 inverted exclamation marka-binaphthyl]ruthenium(II); 142962-95-. Product Category: Ruthenium series catalysts. CAS No. 142962-95-6. Molecular formula: C48H48O4P2Ru. Mole weight: 851.926g/mol. IUPACName: acetic acid;[1-(2-diphenylphosphanyl-5,6,7,8-tetrahydronaphthalen-1-yl)-5,6,7,8-tetrahydronaphthalen-2-yl]-diphenylphosphane;ruthenium. Canonical SMILES: CC(=O)O.CC(=O)O.C1CCC2=C(C1)C=CC(=C2C3=C(C=CC4=C3CCCC4)P(C5=CC=CC=C5)C6=CC=CC=C6)P(C7=CC=CC=C7)C8=CC=CC=C8.[Ru]. Product ID: ACM142962956. Alfa Chemistry ISO 9001:2015 Certified. Categories: (S)-Ru(OAc)2(H8-BINAP | |
| Diacetato[(S)-(-)-2,2'-bis(di-p-tolylphosphino)-1,1'-binaphthyl]ruthenium(II) Ru(OAc)2[(S)-tolbinap] | Diacetato[(S)-(-)-2,2'-bis(di-p-tolylphosphino)-1,1'-binaphthyl]ruthenium(II) Ru(OAc)2[(S)-tolbinap]. Uses: Catalyst system that exhibits high catalytic activity and enantioselectivity in the hydrogenation of enamines. Additional or Alternative Names: 116128-29-1; I14-34252; (S)-Ru(OAc)2(T-BINAP); I14-34094; SC10146; AKOS015908623; Ru[(S)-T-BINAP](OCOCH3)2; (R)-Ru(OAc)2(T-BINAP); MFCD09753021. Product Category: Ruthenium series catalysts. CAS No. 106681-15-6. Molecular formula: C52H48O4P2Ru. Mole weight: 899.97g/mol. IUPACName: acetic acid;[1-[2-bis(4-methylphenyl)phosphanylnaphthalen-1-yl]naphthalen-2-yl]-bis(4-methylphenyl)phosphane;ruthenium. Canonical SMILES: CC1=CC=C(C=C1)P(C2=CC=C(C=C2)C)C3=C(C4=CC=CC=C4C=C3)C5=C(C=CC6=CC=CC=C65)P(C7=CC=C(C=C7)C)C8=CC=C(C=C8)C.CC(=O)O.CC(=O)O.[Ru]. Product ID: ACM106681156. Alfa Chemistry ISO 9001:2015 Certified. | |
| (-)-Dichloro[(4S)-4-(i-propyl)-2-{(S)-2-(diphenylphosphino)ferrocenyl}oxazoline](triphenylphosphine)ruthenium(II) | (-)-Dichloro[(4S)-4-(i-propyl)-2-{(S)-2-(diphenylphosphino)ferrocenyl}oxazoline](triphenylphosphine)ruthenium(II). Uses: Catalyst used for the oxidative kinetic resolution of racemic alcohols. catalyst used for the extremely high enantioselective transfer hydrogenation of ketones and the oxidative kinetic resolution of alcohols. catalyst used for the asymmetric hydrosilylation of ketones and imine. Additional or Alternative Names: Naud Catalyst SK-N003-2z. Product Category: Ruthenium series catalysts. Appearance: orange-brown powder. CAS No. 212133-11-4. Molecular formula: C46H43Cl2FeNOP2Ru. Mole weight: 915.7. Purity: 0.96. IUPACName: (-)-Dichloro[(4S)-4-(i-propyl)-2-{(S)-2-(diphenylphosphino)ferrocenyl}. Product ID: ACM212133114. Alfa Chemistry ISO 9001:2015 Certified. | |
| Dichlorobis(2-(diisopropylphosphino)-ethylamine)ruthenium(II) | Dichlorobis(2-(diisopropylphosphino)-ethylamine)ruthenium(II). Uses: Exceptionally active catalyst for the hydrogenation of ketones and imines under mild conditions. selective hydrogenation of c = o bonds over c = c bonds. Additional or Alternative Names: MFCD07782005; RT-004898; SC10245; Dichlorobis[2-(di-i-propylphosphino)ethylamine]ruthenium (II); Dichlorobis(2-(diisopropylphosphino)-ethylamine)ruthenium(II), 97%; 1092372-90-1. Product Category: Ruthenium series catalysts. CAS No. 1092372-90-1. Molecular formula: C16H40Cl2N2P2Ru. Mole weight: 494.428g/mol. IUPACName: dichlororuthenium;2-di(propan-2-yl)phosphanylethanamine. Canonical SMILES: CC(C)P(CCN)C(C)C.CC(C)P(CCN)C(C)C.Cl[Ru]Cl. Product ID: ACM1092372901. Alfa Chemistry ISO 9001:2015 Certified. | |
| Dichlorobis[2-(di-t-butylphosphino)ethylamine]ruthenium(II), min. 97% | Dichlorobis[2-(di-t-butylphosphino)ethylamine]ruthenium(II), min. 97%. Uses: Exceptionally active catalyst for the hydrogenation of ketones and imines under mild conditions. selective hydrogenation of c = o bonds over c = c bonds. Additional or Alternative Names: 1092372-91-2;Dichlorobis[2-(di-tert-butylphosphino)ethylamine]ruthenium(II);DICHLOROBIS[2-(DI-T-BUTYLPHOSPHINO)ETHYLAMINE]RUTHENIUM(II);Dichlorobis(2-(di-tert-butylphosphino)ethylamine)ruthenium(II), 97%;Dichlorobis[2-(di-tert-butylphosphino)ethylamine]ruthenium(II), 97%;SCHEMBL9939258;MFCD07782003;SC10244;Dichlorobis[2-(di-t-butylphosphino)ethylamine]ruthenium (II). Product Category: Ruthenium series catalysts. CAS No. 1092372-91-2. Molecular formula: C20H48Cl2N2P2Ru. Mole weight: 550.536g/mol. IUPACName: 2-ditert-butylphosphanylethanamine;dichlororuthenium. Canonical SMILES: CC(C)(C)P(CCN)C(C)(C)C.CC(C)(C)P(CCN)C(C)(C)C.Cl[Ru]Cl. Product ID: ACM1092372912. Alfa Chemistry ISO 9001:2015 Certified. | |
| Dichloro[(R)-(+)-2,2',6,6'-tetramethoxy-4,4'-bis(di(3,5-xylyl)phosphino)-3,3'-bipyridine][(1R,2R)-(+)-1,2-diphenylethylenediamine]ruthenium(II), min. 95% | Dichloro[(R)-(+)-2,2',6,6'-tetramethoxy-4,4'-bis(di(3,5-xylyl)phosphino)-3,3'-bipyridine][(1R,2R)-(+)-1,2-diphenylethylenediamine]ruthenium(II), min. 95%. Uses: Effective catalyst for the highly enantioselective hydrogenation of a diverse range of simple aromatic ketones. Additional or Alternative Names: 478308-93-9;MFCD06658135;Dichloro[(R)-(+)-2,2',6,6'-tetramethoxy-4,4'-bis(di(3,5-xylyl)phosphino)-3,3'-bipyridine][(1R,2R)-(+)-1,2-diphenylethylenediamine]ruthenium(II);DICHLORO[(R)-(+)-2,2',6,6'-TETRAMETHOXY-4,4'-BIS(DI(3,5-XYLYL)PHOSPHINO)-3,3'-BIPYRIDINE][(1R,2R)-(+)-1,2-DIPHENYLETHYLENEDIAMINE]RUTHENIUM (II);Dichloro[(R)-4,4'-bis[di(3,5-xylyl)phosphino]-2,2',6,6'-tetramethoxy-3,3'-bipyridine][(R,R)-DPEN]Ru(II). Product Category: Heterocyclic Organic Compound. CAS No. 478308-93-9. Molecular formula: C60H66Cl2N4O4P2Ru. Mole weight: 1141.13g/mol. IUPACName: bis(3,5-dimethylphenyl)-[3-[4-[(2,4-dimethylphenyl)-(3,5-dimethylphenyl)phosphanyl]-2,6-dimethoxypyridin-3-yl]-2,6-dimethoxypyridin-4-yl]phosphane;dichlororuthenium;(1R,2R)-1,2-diphenylethane-1,2-diamine. Canonical SMILES: CC1=CC(=C(C=C1)P(C2=CC(=CC(=C2)C)C)C3=CC(=NC(=C3C4=C(N=C(C=C4P(C5=CC(=CC(=C5)C)C)C6=CC(=CC(=C6)C)C)OC)OC)OC)OC)C.C1=CC=C(C=C1)C(C(C2=CC=CC=C2)N)N.Cl[Ru]Cl. Product ID: ACM478308939. Alfa Chemistry ISO 9001:2015 | |
Our database is helping our users find suppliers everyday.
