Allyl Alcohol Suppliers USA
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Product | Description | |
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Allyl Alcohol Quick inquiry Where to buy Suppliers range | Allyl Alcohol is used in the synthesis of yohimbinoid alkaloids venenatine and alstovenine. Also used in the synthesis of (-)-nakadomarin A, a polycyclic alkaloid. Group: Biochemicals. Alternative Names: 2-Propen-1-ol;1-Hydroxy-2-propene; 1-Propen-3-ol; 2-Propenol; 2-Propenyl Alcohol; 3-Hydroxy-1-propene; 3-Hydroxypropene; Allylic Alcohol; NSC 6526; Shell Unkrauttod A; Vinylcarbinol. Grades: Highly Purified. CAS No. 107-18-6. Pack Sizes: 10g. US Biological Life Sciences. | Worldwide |
Poly(styrene-co-allyl alcohol) Quick inquiry Where to buy Suppliers range | Flexible Organic Transistors. Uses: For analytical and research use. Group: reagents. CAS No. 25119-62-4. | |
Trans-3-(Trimethylsilyl)allyl alcohol Quick inquiry Where to buy Suppliers range | Trans-3-(Trimethylsilyl)allyl alcohol. CAS No: 59376-64-6 | Sarchem Laboratories New Jersey NJ |
1,1'-Bis(diisopropylphosphino)ferrocene Quick inquiry Where to buy Suppliers range | Orange-yellow powder. Uses: Ruthenium- catalyzed hydrohydroxyalkylation of 1,1-disubstituted allenes Ligand for palladium-catalyzed aminocarbonylation of Pyridyl Tosylates by means of ex situ generation of CO. Pd-catalyzed carbonylative ?-arylation of ketones with aryl iodides Ligand for palladium-catalyzed alkoxycarbonylation of aryl bromides for the preparation of tertiary esters Ligand for stereoselective palladium-catalyzed decarboxylative allylation ß-C-glycosylation Ligand for ruthenium-catalyzed C-C coupling reactions of fluorinated alcohols with allenes. Ligand for cobalt-catalyzed intermolecular formal hydroacylation reaction of olefins using N-3-picolin-2-yl aldimines as aldehyde equivalents. Group: Organic Phosphine Compounds. Alternative Names: 1,1-BIS(DIISOPROPYLPHOSPHINO)FERROCENE. Grades: 98%. CAS No. 97239-80-0. Molecular formula: C22H36FeP2. Mole weight: 418.32. IUPAC Name: 1,1-Bis(diisopropylphosphino)ferrocene. Exact Mass: 418.16400. Melting Point: 50-52ºC(lit.). Flash Point: >230 °F. Safty Description: 37/39-26. Hazard statements: Xi: Irritant. | |
1,2-Bis[(2R,5R)-2,5-dimethylphospholano]benzene Quick inquiry Where to buy Suppliers range | 1,2-Bis[(2R,5R)-2,5-dimethylphospholano]benzene. Uses: The DUPHOS family of catalysts is highly efficient for the asymmetric hydrogenation of various substituted cetamidoacrylates and enol acetates yielding products of high enantiomeric excesses. Efficient ligand for the asymmetric hydrogenation of imines, enamines, and enamides. Asymmetric hydrogenation of vinyl alcohols. Catalyst used for the asymmetric hydrogenation of enol phosphonates. Asymmetric hydrogenation of allylic alcohols. Ligand for the catalytic asymmetric [4+1] cycloaddition of vinylallenes with CO. Ligand for the Rh-catalyzed asymmetric enyne cycloisomerization. Catalytic enantioselective addition of dialkylzinc to N-Diphenylphosphinoylimines. Group: Heterocyclic Organic Compound. Alternative Names: (R,R)-1,2-Bis(2,5-dimethylphospholano)benzene; DTXSID20163641; (-)-1,2-Bis[(2R,5R)-2,5-dimethylphospholano]benzene, kanata purity; H5W03D1HAQ; UNII-H5W03D1HAQ; (R,R)-Me-DUPHOS; AJNZWRKTWQLAJK-KLHDSHLOSA-N; (+)-1,2-Bis[(2R,5R)-2,5-dimethylphospholano]benzene; (-)-1,2-Bis((2R,5R)-2,5-dimethylphospholano)benzene; (-)-1,2-Bis[(2R,5R)-2,5-dimethylphospholano]benzene, >=95.0%. CAS No. 147253-67-6. Molecular formula: C18H28P2. Mole weight: 306.37g/mol. IUPAC Name: (2R,5R)-1-[2-[(2R,5R)-2,5-dimethylphospholan-1-yl]phenyl]-2,5-dimethylphospholane. Rotatable Bond Count: 2. Exact Mass: 306.167g/mol. EC Number: 604-579-6. SMILES: CC1CCC(P1C2=CC=CC=C2P3C(CCC3C)C)C. InChI: InChI=1S/C18H28P2/c1-13-9-10-14(2)19(13)17-7-5-6-8-18(17)20-15(3)11-12-16(20)4/h5-8,13-16H,9-12H2,1-4H3/t13-,14-,15-,16-/m1/s1. InChIKey: AJNZWRKTWQLAJK-KLHDSHLOSA-N. Monoisotopic Mass: 306.167g/mol. | |
2,2?-Bis(diphenylphosphino)-1,1?-biphenyl Quick inquiry Where to buy Suppliers range | 2,2?-Bis(diphenylphosphino)-1,1?-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. Mole weight: 522.56. | |
2,2'-Bis(diphenylphosphino)biphenyl Quick inquiry Where to buy Suppliers range | 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. Group: Organic Phosphine Compounds. 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. CAS No. 84783-64-2. Molecular formula: C36H28P2. Mole weight: 522.568g/mol. IUPAC Name: [2-(2-diphenylphosphanylphenyl)phenyl]-diphenylphosphane. Rotatable Bond Count: 7. Exact Mass: 522.167g/mol. 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. InChI: InChI=1S/C36H28P2/c1-5-17-29(18-6-1)37(30-19-7-2-8-20-30)35-27-15-13-25-33(35)34-26-14-16-28-36(34)38(31-21-9-3-10-22-31)32-23-11-4-12-24-32/h1-28H. InChIKey: GRTJBNJOHNTQBO-UHFFFAOYSA-N. Monoisotopic Mass: 522.167g/mol. | |
2,3-Dibromo-1-propanol Quick inquiry Where to buy Suppliers range | 2,3-Dibromo-1-propanol. Uses: Flame Retardant. Group: Brominated Flame Retardant. Alternative Names: DBP; USAF DO-42; Allyl alcohol dibromide; ß-Dibromohydrin; b-Dibromo hydrin; NSC 6203; 1,2-Dibromohydrin; DBP (flame retardant); Dibromopropanol; 2,3-dibromopropan-1-ol; NCI-C55436; 2,3-Dibromopropyl alcohol; Glycerol 1,2-dibromohydrin; beta-dibromohydrin; Brominex 257; ALPHA,BETA-DIBROMOHYDRIN; 1,2-Dibromopropan-3-ol; 2,3-Dibromo-1-propanol; GLYCEROL ALPHA,BETA-DIBROMOHYDRIN; 2,3-Dibromopropanol. CAS No. 96-13-9. Product ID: ACM96139. Molecular formula: C3H6Br2O. Density: 2.12 g/mL at 25 °C. | |
(2E)-3-[4-(Phenylmethoxy)phenyl]-2-propen-1-ol Quick inquiry Where to buy Suppliers range | (2E)-3-[4-(Phenylmethoxy)phenyl]-2-propen-1-ol is used as a regeant in the synthesis for regioselectivity and stereoselective carboxylation of allylic alcohols.1. Group: Biochemicals. Grades: Highly Purified. CAS No. 84184-52-1. Pack Sizes: 10mg, 50mg. Molecular Formula: C16H16O2, Molecular Weight: 240.3. US Biological Life Sciences. | Worldwide |
2-Propen-1,1,2,3,3-d5-1-ol Quick inquiry Where to buy Suppliers range | 2-Propen-1,1,2,3,3-d5-1-ol is isotopically labelled form of Allyl Alcohol, which is used in the synthesis of yohimbinoid alkaloids venenatine and alstovenine. Also used in the synthesis of polycyclic alkaloid (-)-nakadomarin A. Group: Biochemicals. Grades: Highly Purified. CAS No. 102910-30-5. Pack Sizes: 5mg, 10mg. Molecular Formula: C3HD5O. US Biological Life Sciences. | Worldwide |
(2R,5R)-(+)-5-Benzyl-3-methyl-2-(5-methyl-2-furyl)-4-imidazolidinone Quick inquiry Where to buy Suppliers range | (2R,5R)-(+)-5-Benzyl-3-methyl-2-(5-methyl-2-furyl)-4-imidazolidinone is a reactant used in the preparation of allyl heterocycles using palladium-catalyzed allylic amination of allylic alcohols with heterocycles. Group: Biochemicals. Grades: Highly Purified. CAS No. 877303-84-9. Pack Sizes: 50mg, 100mg. Molecular Formula: C16H18N2O2, Molecular Weight: 270.33. US Biological Life Sciences. | Worldwide |
3-Bromo-4-fluoro-5-nitrobenzoic Acid Quick inquiry Where to buy Suppliers range | 3-Bromo-4-fluoro-5-nitrobenzoic Acid is a derivative of m-Nitrobenzoic Acid (N494700), a reagent used in the coupling of allyl acetate to allylic, aliphatic and benzylic alcohols. Group: Biochemicals. Grades: Highly Purified. CAS No. 1290117-21-3. Pack Sizes: 250mg, 500mg. Molecular Formula: C7H3BrFNO4, Molecular Weight: 264.01. US Biological Life Sciences. | Worldwide |
3-Buten-1-ol Quick inquiry Where to buy Suppliers range | 3-Buten-1-ol is an aliphatic primary alcohol used as a reagent in organic synthesis. Group: Biochemicals. Alternative Names: 1-Buten-4-ol; 1-Hydroxy-3-butene; 3-Butenyl Alcohol; 4-Hydroxy-1-butene; Allylcarbinol; Homoallyl Alcohol; NSC 60194; β-Vinylethanol. Grades: Highly Purified. CAS No. 627-27-0. Pack Sizes: 5g. US Biological Life Sciences. | Worldwide |
6-(Allyloxycarbonylamino)-1-hexanol Quick inquiry Where to buy Suppliers range | 6-(Allyloxycarbonylamino)-1-hexanol. Group: Heterocyclic Organic Compound; Amino Alcohols. CAS No. 146292-92-4. Molecular formula: C10H19NO3. Mole weight: 201.26. Symbol: GHS07. Hazard statements: H315-H319-H335. | |
Allyl[1, 3-bis (2, 6-diisopropylphenyl)-2-imidazolidinylidene]chloropalladium (II) Quick inquiry Where to buy Suppliers range | Allyl[1, 3-bis (2, 6-diisopropylphenyl)-2-imidazolidinylidene]chloropalladium (II). Uses: Catalyst for the cross-coupling of aryl chlorides or bromides with aromatic amines. Catalyst for the α-arylation of ketones. Catalyst for anaerobic alcohol oxidation. Group: Heterocyclic Organic Compound. Alternative Names: ALLYLCHLORO[1,3-BIS(2,6-DI-I-PROPYLPHENYL)-4,5-DIHYDROIMIDAZOL-2-YLIDENE]PALLADIUM (II);Allylchloro[1, 3-bis(2, 6-di-i-propylphenyl)-4, 5-dihydroimidazol-2-ylidene]palladium(II), 97%;ALLYLCHLORO[1, 3-BIS-(DIISOPROPYLPHENYL)-2-IMIDAZOLIDINYLIDENE]PALLADIUM(II). Grades: 96%. CAS No. 478980-01-7. Molecular formula: C30H43ClN2Pd. Mole weight: 573.55. IUPAC Name: Allylchloro[1,3-bis(2,6-di-i-propylphenyl)-4,5-dihydroimidazol-2-ylide. Exact Mass: 572.21500. Safty Description: 26-36/37/39. | |
Allyl[1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene]chloropalladium(II) Quick inquiry Where to buy Suppliers range | white solid. Uses: Catalyst for the cross-coupling of aryl chlorides with boronic acids. Catalyst for the diamination of conjugated dienes and trienes. Catalyst for the dehalogenation of aryl chlorides. Catalyst for anaerobic alcohol oxidation. Catalyst for anaerobic ketone oxidation and domino oxidation/α-arylation. Group: Organic Phosphine Compounds. Alternative Names: Palladium, [1,?3-bis[2,?6-bis(1-methylethyl)?phenyl]?-1,?3-dihydro-2H-imidazol-2-ylidene]?chloro(η3-2-propen-1-yl)?-. Grades: 98%, Pd>18.5%. CAS No. 478980-03-9. Molecular formula: C30H42ClN2Pd. Mole weight: 572.54. Symbol: GHS07. Melting Point: > 300 °C (> 572 °F). Hazard statements: H315-H319-H335. | |
Allylbis (2-aminoethyldiphenylphosphino) ruthenium (II) tetrafluoroborate, 98% Quick inquiry Where to buy Suppliers range | Allylbis (2-aminoethyldiphenylphosphino) ruthenium (II) tetrafluoroborate, 98%. Uses: A highly active catalyst for the hydrogenation of amides to alcohols and amines. Catalyst used for the hydrogenation of functionalized amides under basic and neutral conditions. Alternative Names: MFCD30475649; Allylbis (2-aminoethyldiphenylphosphino) ruthenium (II) tetrafluoroborate;1352633-94-3. CAS No. 1352633-94-3. Molecular formula: C31H37BF4N2P2Ru+. Mole weight: 687.472g/mol. IUPAC Name: 2-diphenylphosphanylethanamine;prop-1-ene;ruthenium(2+);tetrafluoroborate. Rotatable Bond Count: 8. Exact Mass: 688.15g/mol. SMILES: [B-](F)(F)(F)F. C=C[CH2]. C1=CC=C(C=C1)P(CCN)C2=CC=CC=C2. C1=CC=C(C=C1)P(CCN)C2=CC=CC=C2. [Ru+2]. InChI: InChI=1S/2C14H16NP.C3H5.BF4.Ru/c2*15-11-12-16(13-7-3-1-4-8-13)14-9-5-2-6-10-14;1-3-2;2-1(3,4)5;/h2*1-10H,11-12,15H2;3H,1-2H2;;/q;;;-1;+2. InChIKey: QUXXWZASZIRDOA-UHFFFAOYSA-N. H-Bond Donor: 2. H-Bond Acceptor: 7. Monoisotopic Mass: 688.15g/mol. | |
Allyl Bromide Quick inquiry Where to buy Suppliers range | Allyl Bromide. Uses: Allyl bromide appears as a clear colorless to light yellow liquid with an irritating unpleasant odor. Flash point 30°F. Irritates eyes, skin, and respiratory system. Toxic by skin absorption. Denser than water and slightly soluble in water.;Liquid. Group: Polymerization Reagents. CAS No. 106-95-6. IUPAC Name: 3-bromoprop-1-ene. Molecular Weight: 120.98g/mol. Molecular Formula: C3H5Br. SMILES: C=CCBr. InChI: InChI=1S/C3H5Br/c1-2-3-4/h2H,1,3H2. InChIKey: BHELZAPQIKSEDF-UHFFFAOYSA-N. Boiling Point: 158 °F at 760 mm Hg (USCG, 1999);70.1 ?;71.3 ? at 760 mm Hg. Melting Point: -182 °F (USCG, 1999);-119.0 ?;-119 ?. Flash Point: 28 °F (USCG, 1999);30 °F (-1 ?). Density: 1.4161 at 68 °F (USCG, 1999);1.398 at 20 ?/4 ?. Solubility: 0.03 M;Miscible with alcohol, chloroform, ether, carbon disulfide, carbon tetrachloride;In water, 3,835 mg/L at 25 ?. | |
Allyloxytrimethylsilane Quick inquiry Where to buy Suppliers range | Transparent liquid. Group: Alkenes. Alternative Names: Allyl trimethylsilyl ether; Allyloxytrimethylsilane; trimethylallyloxysilane; AllyloxytriMethylsilane; O-(trimethylsilyl)allyl alcohol; 3-trimethylsiloxy-1-propene; 3-(Trimethylsiloxy)propene; Trimethyl(2-propenyloxy)silane; (2-propenyloxy)trimethylsilane. Grades: 95%+. CAS No. 18146-00-4. Molecular formula: C7H5ClO. Mole weight: 130.26. IUPAC Name: trimethyl(prop-2-enoxy)silane. Exact Mass: 130.08100. Symbol: GHS02. EC Number: 242-031-4. Boiling Point: 100-102ºC(lit.). Flash Point: 31 °F. Density: 0.773 g/mL at 25ºC(lit.). SMILES: C[Si](C)(C)OCC=C. InChIKey: MNMVKGDEKPPREK-UHFFFAOYSA-N. Safty Description: 16-26-36. Hazard statements: H226-H319. | |
Bis (benzonitrile)dichloroplatinum (II) Quick inquiry Where to buy Suppliers range | Bis (benzonitrile)dichloroplatinum (II). Uses: Catalyst for: Asymmetric hydroformylation reactions Allylation reactions Carbene insertion into O-H bonds of alcohols Cyclopropanation reactions Hydrosilylation reacttions. Group: Platinum series of catalysts. Alternative Names: AKOS015964364; cis-Di(benzonitrile)dichloroplatinum (II); 15617-19-3; dichloride; AC1L38NI. CAS No. 15617-19-3. Molecular formula: C14H10Cl2N2Pt. Mole weight: 472.232g/mol. IUPAC Name: benzonitrile; platinum(2+); dichloride. Exact Mass: 470.987g/mol. EC Number: 238-943-7. SMILES: C1=CC=C(C=C1)C#N. C1=CC=C(C=C1)C#N. [Cl-]. [Cl-]. [Pt+2]. InChI: InChI=1S/2C7H5N.2ClH.Pt/c2*8-6-7-4-2-1-3-5-7;;;/h2*1-5H;2*1H;/q;;;;+2/p-2. InChIKey: WAJRCRIROYMRKA-UHFFFAOYSA-L. H-Bond Acceptor: 4. Monoisotopic Mass: 470.987g/mol. | |
Bis(dibenzylideneacetone)palladium, Pd : 18.4 wt.% Quick inquiry Where to buy Suppliers range | Bis(dibenzylideneacetone)palladium (Pd(dba)2) is an air-stable Pd0 complex. It is a reagent for the synthesis of allyl-substituted cyclopentadiene. It is a homogeneous catalyst that can catalyze the alkylation of allyl acetate by the action of various nucleophiles under mild conditions. Uses: ·Synthesis of isomer 2-aryl-2,5-dihydrofuran by Heck coupling reaction of aryl bromide with alkene using neopentylphosphine ligand; ·Heck reaction of benzyl trifluoroacetate and 2,3-dihydrofuran phosphoramidite ligand; ·Allylation of stable anions; ·Cross-coupling of allyl, alkenyl and aryl halides with organotin compounds; ·Cross-coupling of vinyl halides with alkenyl zinc compounds; ·Carbonylation of alkenyl and aryl halides; ·Efficient oxidation of alcohols to aldehydes and ketones together with cyclic thiourea ligands. Group: Colloidal Catalysts. CAS No. 32005-36-0. Molecular Weight: 575 g/mol. SMILES: [Pd]. O=C(/C=C/c1ccccc1)\C=C\c2ccccc2. O=C(/C=C/c3ccccc3)\C=C\c4ccccc4. InChI: UKSZBOKPHAQOMP-SVLSSHOZSA-N. Boiling Point: 150 °C. | |
Bis(pyridine)(1,5-cyclooctadiene)iridium(I) hexafluorophosphate, 99% Quick inquiry Where to buy Suppliers range | Bis(pyridine)(1,5-cyclooctadiene)iridium(I) hexafluorophosphate, 99%. Uses: This complex is used in the isomerization of primary allylic alcohols. The catalyst is used for ortho-directed hydrogen-isotope exchange. CAS No. 56678-60-5. Molecular formula: C18H22F6IrN2P. Mole weight: 603.56. | |
Carbonylchlorohydridotris (triphenylphosphine)ruthenium (II) Quick inquiry Where to buy Suppliers range | Carbonylchlorohydridotris (triphenylphosphine)ruthenium (II). Uses: Catalyst for alcohol α-allylation with dienes or allenes under transfer hydrogenation conditions. Catalyst for tandem isomerization (to imine), followed by Friedel Crafts alkylation. Catalyst for amination of alcohols with ammonia. Group: Ruthenium series catalysts. Alternative Names: Carbonylchlorohydridotris (triphenylphosphine)ruthenium (II); 16971-33-8; MFCD00049804; Ru (CO)ClH[P (C6H5)3]3; [ (C6H5)3P]3Ru (CO) (Cl)H; AKOS024258164. CAS No. 16971-33-8. Molecular formula: C55H48ClOP3Ru. Mole weight: 954.429g/mol. IUPAC Name: chloro(hydrido)ruthenium; formaldehyde; triphenylphosphane. Rotatable Bond Count: 9. Exact Mass: 954.165g/mol. EC Number: 241-051-0. 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]. InChI: InChI=1S/3C18H15P.CH2O.ClH.Ru.H/c3*1-4-10-16(11-5-1)19(17-12-6-2-7-13-17)18-14-8-3-9-15-18;1-2;;;/h3*1-15H;1H2;1H;;/q;;;;;+1;/p-1. InChIKey: IOCHTJOKPQTFJY-UHFFFAOYSA-M. H-Bond Acceptor: 1. Monoisotopic Mass: 954.165g/mol. | |
Chloro[1,3-bis(t-butyl)-2H-imidazol-2-ylidene]gold(I), 98% Quick inquiry Where to buy Suppliers range | Chloro[1,3-bis(t-butyl)-2H-imidazol-2-ylidene]gold(I), 98%. Uses: Catalyst for the rearrangement of allylic acetates Catalyst for the α-allylation of enals and enones with alcohols. Alternative Names: MFCD29037187;Chloro[1,3-bis(1,1'-dimethylethyl)2H-imidazol-2-ylidene]gold(I);839722-07-5. CAS No. 839722-07-5. Molecular formula: C11H20AuClN2. Mole weight: 412.712g/mol. IUPAC Name: chloro-(1,3-ditert-butylimidazol-2-ylidene)gold. Rotatable Bond Count: 2. Exact Mass: 412.098g/mol. SMILES: CC(C)(C)N1C=CN(C1=[Au]Cl)C(C)(C)C. InChI: InChI=1S/C11H20N2.Au.ClH/c1-10(2,3)12-7-8-13(9-12)11(4,5)6;;/h7-8H,1-6H3;;1H/q;+1;/p-1. InChIKey: OZAGJDJSGBJLSH-UHFFFAOYSA-M. H-Bond Acceptor: 2. Monoisotopic Mass: 412.098g/mol. | |
Cobalt(II) ethyl/butyl phosphonate Silica (PhosphonicS POCo) Quick inquiry Where to buy Suppliers range | Cobalt(II) ethyl/butyl phosphonate Silica (PhosphonicS POCo). Uses: Catalyst used for oxidation of a wide variety allylic alcohols and alkene substrates, including complex steroids. | |
Dichloro[(2,6,10-dodecatriene)-1,12-diyl]ruthenium(IV) Quick inquiry Where to buy Suppliers range | Dichloro[(2,6,10-dodecatriene)-1,12-diyl]ruthenium(IV). Uses: An efficient catalyst used for the isomerization of allylic alcohols into carbonyl compounds in organic or aqueous media. An efficient catalyst used for the deprotection of N-allylic amines. Alternative Names: Dichloro(2,6,10-dodecatriene-1,12-diyl)ruthenium(IV). CAS No. 12170-97-7. Product ID: ACM12170977-1. Molecular formula: C12H18Cl2Ru. Mole weight: 334.24. Appearance: Orange xtl. | |
Manganese(IV) Oxide Quick inquiry Where to buy Suppliers range | Manganese(IV) Oxide is used in dry-cell batteries such as alkaline battery and the zinc-carbon battery. It is also used in the oxidation of allylic alcohols. Group: Biochemicals. Grades: Highly Purified. CAS No. 1313-13-9. Pack Sizes: 25g, 100g. Molecular Formula: MnO2, Molecular Weight: 86.94. US Biological Life Sciences. | Worldwide |
[NH2Me2][(RuCl((R)-binap))2(μ-Cl)3] Quick inquiry Where to buy Suppliers range | [NH2Me2][(RuCl((R)-binap))2(μ-Cl)3]. Uses: (R)-BINAP or (R)-Tol-BINAP can be combined with dichloro(1,5-cyclooctadiene)ruthenium to form precursors to NOYORI CATALYST SYSTEMS. These systems exhibit very high catalytic activity and enantioselectivity in the hydrogenation of a wide range of substrates. NOYORI CATALYST SYSTEMS have been shown to effect highly enantioselective hydrogenation of functionalized ketones where the substituents are dialkylamino, hydroxy, siloxy, carbonyl, ester, amide or thioester. Useful ligand in asymmetric Heck processes. Ligand employed in palladium-catalyzed asymmetric arylation of ketones. Ligand employed in rhodium-catalyzed 1,4-additions to enones. Ligand employed in palladium-catalyzed hydroamination of styrene derivatives. Ligand employed in silver-catalyzed asymmetric Sakuri-Hosomi allylation and Mukaiyama aldol reaction. Ligand employed in rhodium-catalyzed kinetic resolution of enynes. Ligand employed in asymmetric rhodium-catalyzed hydroboration of cyclopropenes. Ligand employed in silver-catalyzed a-hydroxylation of stannyl enol ethers. Ligand employed in palladium-catalyzed synthesis of chiral allenes. Ligand for palladium-catalyzed enantioselective hetero Michael addition to form b-amino acid derivatives. Ligand employed in rhodium-catalyzed asymmetric rearrangement of alkynyl alkenyl carbinols. Ligand employed in rhodium-catalyzed 1,2-addition of aluminium organyl compounds to cyclic enones. Ligand employed in iridium-catalyzed transfer hydrogenative allylation of benzylic alcohols. Ligand employed in rhodium-catalyzed asymmetric C-Si bond formation by conjugate silyl transfer using a Si-B linkage. Group: Ruthenium series catalysts. Alternative Names: J-012887; (R)-[(RuCl(BINAP))2( -Cl)3][NH2Me2]; DIMETHYLAMMONIUM DICHLOROTRI(MU-CHLORO)BIS[(R)-(+)-2,2'-BIS(DIPHENYLPHOSPHINO)-1,1'-BINAPHTHYL]DIRUTHENATE(II); 199684-47-4; 199541-17-8; Dimethylammonium dichlorotri(mu-chloro)bis[(R)-(+)-2,2'-bis(diphenylphosphino)-1,1'-binaphthyl]diruthenate(II), [NH2Me2][{RuCl((R)-binap)}2(mu-Cl)3]; (R)-[(RuCl(BINAP))2(mu-Cl)3[NH2Me2]; DIMETHYLAMMONIUM DICHLOROTRI(MU-CHLORO)BIS[(S)-(-)-2,2'-BIS(DIPHENYLPHOSPHINO)-1,1'-BINAPHTHYL]DIRUTHENATE(II); (R)-[(RuCl(BINAP))2(|I-Cl)3[NH2Me2]. CAS No. 199684-47-4. Molecular formula: C90H75Cl5NP4Ru | |
[NH2Me2][(RuCl((S)-binap))2(μ-Cl)3] Quick inquiry Where to buy Suppliers range | [NH2Me2][(RuCl((S)-binap))2(μ-Cl)3]. Uses: (R)-BINAP or (R)-Tol-BINAP can be combined with dichloro(1,5-cyclooctadiene)ruthenium to form precursors to NOYORI CATALYST SYSTEMS. These systems exhibit very high catalytic activity and enantioselectivity in the hydrogenation of a wide range of substrates. NOYORI CATALYST SYSTEMS have been shown to effect highly enantioselective hydrogenation of functionalized ketones where the substituents are dialkylamino, hydroxy, siloxy, carbonyl, ester, amide or thioester. Useful ligand in asymmetric Heck processes. 3. Ligand employed in palladium-catalyzed asymmetric arylation of ketones. 4. Ligand employed in rhodium-catalyzed 1,4-additions to enones. 5. Ligand employed in palladium-catalyzed hydroamination of styrene derivatives. 6. Ligand employed in silver-catalyzed asymmetric Sakuri-Hosomi allylation and Mukaiyama aldol reaction. 7. Ligand employed in rhodium-catalyzed kinetic resolution of enynes. 8. Ligand employed in asymmetric rhodium-catalyzed hydroboration of cyclopropenes. 9. Ligand employed in silver-catalyzed a-hydroxylation of stannyl enol ethers. 10. Ligand employed in palladium-catalyzed synthesis of chiral allenes. 11. Ligand for palladium-catalyzed enantioselective hetero Michael addition to form b-amino acid derivatives. 12. Ligand employed in rhodium-catalyzed asymmetric rearrangement of alkynyl alkenyl carbinols. 13. Ligand employed in rhodium-catalyzed 1,2-addition of aluminium organyl compounds to cyclic enones. 14. Ligand employed in iridium-catalyzed transfer hydrogenative allylation of benzylic alcohols. 15. Ligand employed in rhodium-catalyzed asymmetric C-Si bond formation by conjugate silyl transfer using a Si-B linkage. Group: Ruthenium series catalysts. Alternative Names: (S)-[(RuCl(BINAP))2( -Cl)3][NH2Me2]; Dimethylammonium dichlorotri(mu-chloro)bis[(R)-(+)-2,2'-bis(diphenylphosphino)-1,1'-binaphthyl]diruthenate(II), [NH2Me2][{RuCl((R)-binap)}2(mu-Cl)3]; (S)-[(RUCL(BINAP))2(MU-CL)3][NH2ME2]; [NH2ME2][[RUCL((S)-BINAP)]2(MU-CL)3]; (R)-[(RuCl(BINAP))2(mu-Cl)3[NH2Me2]; Dimethylammonium dichlorotri(|I-chloro)bis[(S)-(-)-2,2 inverted exclamation marka-bis(diphenylphosphino)-1,1 inverted exclamation marka-binaphthyl]diruthenate(II); Dimethylammonium dichlorotri(|I-chloro)bis[(R)-(+)-2,2 inverted ex | |
poly(allylamine) Quick inquiry Where to buy Suppliers range | poly(allylamine). Uses: Allylamine appears as a colorless to light yellow colored liquid with a strong ammonia-like odor. Less dense than water. Vapors are heavier than air. Toxic by inhalation, ingestion and skin absorption. Irritates skin, eyes and mucous membranes. Flash point below 0°F. Boiling point 130°F. Used to make pharmaceuticals and other chemicals.;Liquid;COLOURLESS-TO-YELLOW LIQUID WITH PUNGENT ODOUR. Group: Polymers. CAS No. 30551-89-4. IUPAC Name: prop-2-en-1-amine. Molecular Weight: 57.09g/mol. Molecular Formula: C3H7N;CH2CHCH2NH2;C3H7N. SMILES: C=CCN. InChI: InChI=1S/C3H7N/c1-2-3-4/h2H,1,3-4H2. InChIKey: VVJKKWFAADXIJK-UHFFFAOYSA-N. Boiling Point: 131 to 136 °F at 760 mm Hg (EPA, 1998);53.3 ?;53.5 ?;52-53 ?. Melting Point: -126 °F (NTP, 1992);-88.2 ?;-88.2 ?;-88 ?. Flash Point: -20 °F (EPA, 1998);-29 ? (-20 °F) - closed cup;10 °F (-12 ?) - closed cup;-29 ? c.c. Density: 0.76 at 68 °F (EPA, 1998);0.760 at 20 ?/20 ?;Relative density (water = 1): 0.8. Solubility: Very soluble (NTP, 1992);17.51 M;In water, 1X10+6 mg/L at 20 ? /miscible/;Miscible with water;Miscible with alcohol, chloroform, ether;Solubility in water: miscible. Viscosity: 0.3745 Poise. | |
Poly(allylamine) solution Quick inquiry Where to buy Suppliers range | Poly(allylamine) solution. Uses: Allylamine appears as a colorless to light yellow colored liquid with a strong ammonia-like odor. Less dense than water. Vapors are heavier than air. Toxic by inhalation, ingestion and skin absorption. Irritates skin, eyes and mucous membranes. Flash point below 0°F. Boiling point 130°F. Used to make pharmaceuticals and other chemicals.;Liquid;COLOURLESS-TO-YELLOW LIQUID WITH PUNGENT ODOUR. Group: Hydrophilic Polymers. CAS No. 30551-89-4. IUPAC Name: prop-2-en-1-amine. Molecular Weight: 57.09g/mol. Molecular Formula: C3H7N;CH2CHCH2NH2;C3H7N. SMILES: C=CCN. InChI: InChI=1S/C3H7N/c1-2-3-4/h2H,1,3-4H2. InChIKey: VVJKKWFAADXIJK-UHFFFAOYSA-N. Boiling Point: 131 to 136 °F at 760 mm Hg (EPA, 1998);53.3 ?;53.5 ?;52-53 ?. Melting Point: -126 °F (NTP, 1992);-88.2 ?;-88.2 ?;-88 ?. Flash Point: -20 °F (EPA, 1998);-29 ? (-20 °F) - closed cup;10 °F (-12 ?) - closed cup;-29 ? c.c. Density: 0.76 at 68 °F (EPA, 1998);0.760 at 20 ?/20 ?;Relative density (water = 1): 0.8. Solubility: Very soluble (NTP, 1992);17.51 M;In water, 1X10+6 mg/L at 20 ? /miscible/;Miscible with water;Miscible with alcohol, chloroform, ether;Solubility in water: miscible. Viscosity: 0.3745 Poise. | |
(R) -1-[ (SP) -2- (Dicyclohexylphosphino) ferrocenyl]ethyldi-tert-butylphosphine Quick inquiry Where to buy Suppliers range | (R) -1-[ (SP) -2- (Dicyclohexylphosphino) ferrocenyl]ethyldi-tert-butylphosphine. Uses: Ligand for Palladium-catalyzed C-N cross-coupling. Ligand for Palladium-catalyzed C-S cross-coupling. Ligand for Palladium-catalyzed Kumada couplings of aryl and vinyl tosylates. Ligand for Rhodium-catalyzed hydroacylation of cyclopropenes, an enatioselective desymmetrization method. Ligand for Palladium-catalyzed C-O cross-coupling. Ligand for Rhodium-catalyzed coupling of imidazole derivatives with terminal allenes. Ligand for Ruthenium-catalyzed C-C coupling of alkynes and alcohols to form branched products of carbonyl allylation. CAS No. 158923-11-6. Molecular formula: C32H52FeP2 10*. Mole weight: 554.55. | |
(R)-(+)-2-Diphenylphosphino-2'-methoxy-1,1'-binaphthyl Quick inquiry Where to buy Suppliers range | (R)-(+)-2-Diphenylphosphino-2'-methoxy-1,1'-binaphthyl. Uses: 1. Efficient catalyst for the enantoselective hydrosilyation of 1-alkenes to optically active 2-alcohols. 2. Ligand for palladium-catalyzed asymmetric reduction of allyltc esters. 3. Ligand for the rhodium-catalyzed asymmetric aryiation of imines with organostannanes. 4. Ligand for the rhodiunvcatalyzed asymmetrk: addition of aryl- and alkenyiborontc acids to Isatins. 5. Ligand for desymmetrizatlon of malonamides via an enantiosetective intramolecular Buchwatd-Hartwig reaction. Group: Heterocyclic Organic Compound. CAS No. 145964-33-6. Molecular formula: C33H25OP. Mole weight: 468.536g/mol. IUPAC Name: [1-(2-methoxynaphthalen-1-yl)naphthalen-2-yl]-diphenylphosphane. Rotatable Bond Count: 5. Exact Mass: 468.164g/mol. SMILES: COC1=C (C2=CC=CC=C2C=C1)C3=C (C=CC4=CC=CC=C43)P (C5=CC=CC=C5)C6=CC=CC=C6. InChI: InChI=1S/C33H25OP/c1-34-30-22-20-24-12-8-10-18-28(24)32(30)33-29-19-11-9-13-25(29)21-23-31(33)35(26-14-4-2-5-15-26)27-16-6-3-7-17-27/h2-23H,1H3. InChIKey: KRWTWSSMURUMDE-UHFFFAOYSA-N. H-Bond Acceptor: 1. Monoisotopic Mass: 468.164g/mol. | |
[(R)-(+)-5,5'-Bis(diphenylphosphino)-4,4'-bi-1,3-benzodioxole][4-cyano-3-nitrobenzenecarboxylato][1,2,3-n-2-propenyl]iridium(III), min. 97% Quick inquiry Where to buy Suppliers range | [(R)-(+)-5,5'-Bis(diphenylphosphino)-4,4'-bi-1,3-benzodioxole][4-cyano-3-nitrobenzenecarboxylato][1,2,3-n-2-propenyl]iridium(III), min. 97%. Uses: Catalyst used for the diastereo- and enantioselective carbonyl (trimethylsilyl)allylation from the alcohol, or aldehyde, oxidation level. Catalyst used for the diastereo- and enantioselective carbonyl (hydroxy)allylation to form anti-1,2-diols. Catalyst used for the diastereo- and enantioselective carbonyl (hydroxymethyl)allylation from the alcohol, or aldehyde, oxidation level. Catalyst used for the diastereo- and enantioselective carbonyl tert-prenylation from the alcohol, or aldehyde, oxidation level. Catalyst used for the diastereo- and enantioselective carbonyl double crotylation of 1,3-diols. Catalyst used for the diastereo- and enantioselective carbonyl crotylation from the alcohol or aldehyde oxidation level. Alternative Names: MFCD20922908;Krische Ir Catalyst: (S)-SEGPHOS, 4-cyano-3-nitrobenzoate ligated, AldrichCPR;[(R)-(+)-5,5'-Bis(diphenylphosphino)-4,4'-bi-1,3-benzodioxole][4-cyano-3-nitrobenzenecarboxylato][1,2,3- -2-propenyl]Ir(III);[(R)-5,5'-Bis(diphenylphosphino)-4,4'-bi-1,3-benzodioxole][4-cyano-3-nitrobenzenecarboxylato][1,2,3--2-propenyl]Ir(III);1208092-27-6. CAS No. 1208092-27-6. Molecular formula: C49H36IrN2O8P2-. Mole weight: 1034.998g/mol. IUPAC Name: 4-cyano-3-nitrobenzene-6-ide-1-carboxylic acid;[4-(5-diphenylphosphanyl-1,3-benzodioxol-4-yl)-1,3-benzodioxol-5-yl]-diphenylphosphane;iridium;propane. Rotatable Bond Count: 7. Exact Mass: 1035.158g/mol. SMILES: [CH2][CH][CH2]. C1OC2=C (O1)C (=C (C=C2)P (C3=CC=CC=C3)C4=CC=CC=C4)C5=C (C=CC6=C5OCO6)P (C7=CC=CC=C7)C8=CC=CC=C8. C1=[C-]C (=CC (=C1C#N)[N+] (=O)[O-])C (=O)O. [Ir]. InChI: InChI=1S/C38H28O4P2. C8H3N2O4. C3H5. Ir/c1-5-13-27(14-6-1)43(28-15-7-2-8-16-28)33-23-21-31-37(41-25-39-31)35(33)36-34(24-22-32-38(36)42-26-40-32)44(29-17-9-3-10-18-29)30-19-11-4-12-20-30; 9-4-6-2-1-5(8(11)12)3-7(6)10(13)14; 1-3-2; /h1-24H, 25-26H2; 2-3H, (H, 11, 12); 3H, 1-2H2; /q; -1; ;. InChIKey: WNUGBSVEKALVKR-UHFFFAOYSA-N. H-Bond Donor: 1. H-Bond Acceptor: 10. Monoisotopic Mass: 1035.158g/mol. | |
(R)-(+)-BINAP Quick inquiry Where to buy Suppliers range | (R)-(+)-BINAP. Uses: (R)-BINAP or (R)-Tol-BINAP can be combined with dichloro(1,5-cyclooctadiene)ruthenium to form precursors to NOYORI CATALYST SYSTEMS. These systems exhibit very high catalytic activity and enantioselectivity in the hydrogenation of a wide range of substrates. NOYORI CATALYST SYSTEMS have been shown to effect highly enantioselective hydrogenation of functionalized ketones where the substituents are dialkylamino, hydroxy, siloxy, carbonyl, ester, amide or thioester. Useful ligand in asymmetric Heck processes. Ligand employed in palladium-catalyzed asymmetric arylation of ketones. Ligand employed in rhodium-catalyzed 1,4-additions to enones. Ligand employed in palladium-catalyzed hydroamination of styrene derivatives. Ligand employed in silver-catalyzed asymmetric Sakuri-Hosomi allylation and Mukaiyama aldol reaction. Ligand employed in rhodium-catalyzed kinetic resolution of enynes. Ligand employed in asymmetric rhodium-catalyzed hydroboration of cyclopropenes. Ligand employed in silver-catalyzed a-hydroxylation of stannyl enol ethers. Ligand employed in palladium-catalyzed synthesis of chiral allenes. Ligand for palladium-catalyzed enantioselective hetero Michael addition to form b-amino acid derivatives. Ligand employed in rhodium-catalyzed asymmetric rearrangement of alkynyl alkenyl carbinols. Ligand employed in rhodium-catalyzed 1,2-addition of aluminium organyl compounds to cyclic enones. Ligand employed in iridium-catalyzed transfer hydrogenative allylation of benzylic alcohols. Ligand employed in rhodium-catalyzed asymmetric C-Si bond formation by conjugate silyl transfer using a Si-B linkage. Ligand employed in the iridium-catalyzed asymmetric cyclopropane-mediated carbonyl allylation of primary alcohols. Ligand employed in the nickel-catalyzed asymmetric α-arylation of tetralones. Ligand employed in the copper-catalyzed asymmetric propargylation of ketones. Ligand employed in the cobalt-catalyzed asymmetric reductive coupling of alkynes with alkenes. Ligand employed in the rhodium-catalyzed asymmetric 1,4-addition of arylalanes on trisubstituted enones. Ruthenium-catalyzed asymmetric hydrocyanation of imines. Palladium-catalyzed asymmetric intermolecular cyclization. Group: Organic Phosphine Compounds. Alternative Names: -Bis(d | |
Rhodium(II) Acetate Dimer Quick inquiry Where to buy Suppliers range | Rhodium(II) Acetate Dimer. Uses: Catalyst for insertion into C-H and X-H bonds. Catalyst for Ylide generation. Doyle-Kirmse Reaction of Allylic Sulfides with Diazoalkane Claisen rearrangement. Epoxides from aldehydes. Synthesis of aziridines from allylic N-tosyloxycarbamates. Rh/NHC catalyzed direct intermolecular arylation of C-H bonds. Chiral Bronsted acid-Rh catalyzed three component reactions of diazo compounds with alcohols and imines. Rh-catalyzed cyclopropenations of ynamides. Tandem asymmetric aza-Darzens/ring-opening reactions. Group: Micro/NanoElectronics. Alternative Names: Dirhodium tetraacetate; Rhodium(II) acetate, dimer, Premion®; Rhodium, tetrakis(mu-acetato)di-; Rhodium acetate, dimer; Rhodium(II) acetate dimer; Tetrakis(mu-(acetato-O:O'))dirhodium; A830446; SY010327; SC-26584; TETRAKIS(ACETO)DIRHODIUM(II). CAS No. 15956-28-2. Molecular formula: C8H12O8Rh2. Mole weight: 441.987g/mol. IUPAC Name: rhodium(2+);tetraacetate. Exact Mass: 441.864g/mol. EC Number: 240-084-8. SMILES: CC(=O)[O-].CC(=O)[O-].CC(=O)[O-].CC(=O)[O-].[Rh+2].[Rh+2]. InChI: InChI=1S/4C2H4O2.2Rh/c4*1-2(3)4;;/h4*1H3,(H,3,4);;/q;;;;2*+2/p-4. InChIKey: SYBXSZMNKDOUCA-UHFFFAOYSA-J. H-Bond Acceptor: 8. Monoisotopic Mass: 441.864g/mol. | |
(S)-(-)-2-Diphenylphosphino-2'-methoxy-1,1'-binaphthyl Quick inquiry Where to buy Suppliers range | (S)-(-)-2-Diphenylphosphino-2'-methoxy-1,1'-binaphthyl. Uses: Efficient catalyst for the enantioselective hydrosilyation of 1-alkenes to optically active 2-alcohols. Ligand for palladium-catalyzed asymmetric reduction of allylic esters. Ligand for the rhodium-catalyzed asymmetric arylation of imines with organostannanes. Ligand for the rhodium-catalyzed asymmetric addition of aryland alkenylboronic acids to Isatins. Group: Heterocyclic Organic Compound. CAS No. 134484-36-9. Molecular formula: C33H25OP. Mole weight: 468.536g/mol. IUPAC Name: [1-(2-methoxynaphthalen-1-yl)naphthalen-2-yl]-diphenylphosphane. Rotatable Bond Count: 5. Exact Mass: 468.164g/mol. SMILES: COC1=C (C2=CC=CC=C2C=C1)C3=C (C=CC4=CC=CC=C43)P (C5=CC=CC=C5)C6=CC=CC=C6. InChI: InChI=1S/C33H25OP/c1-34-30-22-20-24-12-8-10-18-28(24)32(30)33-29-19-11-9-13-25(29)21-23-31(33)35(26-14-4-2-5-15-26)27-16-6-3-7-17-27/h2-23H,1H3. InChIKey: KRWTWSSMURUMDE-UHFFFAOYSA-N. H-Bond Acceptor: 1. Monoisotopic Mass: 468.164g/mol. | |
[(S)-(-)-5,5'-Bis(diphenylphosphino)-4,4'-bi-1,3-benzodioxole][4-cyano-3-nitrobenzenecarboxylato][1,2,3-η-2-propenyl]iridium(III), min. 97% Quick inquiry Where to buy Suppliers range | [(S)-(-)-5,5'-Bis(diphenylphosphino)-4,4'-bi-1,3-benzodioxole][4-cyano-3-nitrobenzenecarboxylato][1,2,3-η-2-propenyl]iridium(III), min. 97%. Uses: 1. Catalyst used for the diastereo- and enantioselective carbonyl (trimethylsilyl)allylation from the alcohol, or aldehyde, oxidation level. 2. Catalyst used for the diastereo- and enantioselective carbonyl (hydroxy)allylation to form anti-1,2-diols. 3. Catalyst used for the diastereo- and enantioselective carbonyl (hydroxymethyl)allylation from the alcohol, or aldehyde, oxidation level. 4. Catalyst used for the diastereo- and enantioselective carbonyl tert-prenylation from the alcohol, or aldehyde, oxidation level. 5. Catalyst used for the diastereo- and enantioselective carbonyl double crotylation of 1,3-diols. 6. Catalyst used for the diastereo- and enantioselective carbonyl crotylation from the alcohol or aldehyde oxidation level. Group: Heterocyclic Organic Compound. CAS No. 1221768-92-8. Molecular formula: C49H35IrN2O8P2. Mole weight: 1033.98. | |
Silver Trifluoromethanesulfonate Quick inquiry Where to buy Suppliers range | Silver Trifluoromethanesulfonate. Uses: Silver precatalyst for the asymmetric allylation of aldehydes Silver catalyst for intramolecular additions of alcohols and carboxylic acids to inert olefins Silver catalyst for the fluorination of boronic acids Silver catalyst for the fluorination of functionalized aryl stannanes Silver catalyst for cyclopropenation of internal alkynes with donor/acceptor substituted diazo compounds Silver catalyst for the reaction of 2-alkynylbenzaldehyde with 2-isocyanoacetate. Group: Silver series of catalysts. Alternative Names: KSC491Q9D; Silver trifluoromethanesulfonate, >=99%; silver(1+) ion trifluoromethanesulfonate; silver(i)trifluoromethanesulfonate; TRIFLUOROMETHANESULFONATE SILVER SALT; trifluormethanesulfonic acid silver salt; silver(i) trifluoromethanesulphonate; ANW-26574; QRUBYZBWAOOHSV-UHFFFAOYSA-M; X7226. CAS No. 2923-28-6. Molecular formula: CAgF3O3S. Mole weight: 256.931g/mol. IUPAC Name: silver;trifluoromethanesulfonate. Exact Mass: 255.857g/mol. EC Number: 220-882-2. SMILES: C(F)(F)(F)S(=O)(=O)[O-].[Ag+]. InChI: InChI=1S/CHF3O3S.Ag/c2-1(3,4)8(5,6)7;/h(H,5,6,7);/q;+1/p-1. InChIKey: QRUBYZBWAOOHSV-UHFFFAOYSA-M. | |
Styrene/allyl alcohol copolymer Quick inquiry Where to buy Suppliers range | Styrene/allyl alcohol copolymer. Group: Polymer/Macromolecule. Alternative Names: 2-Propen-1-ol, polymerwithethenylbenzene; Aeroleinpolymerwithstyrene; POLY(STYRENE-CO-ALLYL ALCOHOL);SAA-100(TM), SAA-101(TM);STYRENE/ALLYL ALCOHOL COPOLYMER;STYRENE-ALLYL ALCOHOL COPOLYMERS;2-Propen-1-ol/styrene copolymer;SAA 100. CAS No. 25119-62-4. Molecular formula: C33H42O3X2. Mole weight: 2800. Flash Point: >200°F. Density: 1.05 (20°C). | |
t-BuDavePhos Quick inquiry Where to buy Suppliers range | t-BuDavePhos. Uses: Useful ligand for Pd-catalyzed carbon-oxygen bond forming reactions. Ligand used selective Pd-catalyzed arylation of ammonia. Application to the synthesis of dibenzodiazepines. Ligand used for selective Pd-catalyzed silylation of aryl chlorides. Ligand used for Pd(0)-catalyzed direct dehydrative coupling of terminal alkynes with allylic alcohols to access 1,4-enynes. Group: Organic Phosphine Compounds. Alternative Names: 2 inverted exclamation marka-(Di-tert-butylphosphino)-N,N-dimethylbiphenyl-2-amine; SCHEMBL238097; t-BuDavePhos, 97%; 2-di(tert-butyl)phosphino-2'-(N,N-dimethylamino)biphenyl; AB0005790; J3.548.578C; MFCD03426986; tBuDavePhos; [2'-(DI-TERT-BUTYL-PHOSPHANYL)-BIPHENYL-2-YL]-DIMETHYL-AMINE; SC-73179. CAS No. 224311-49-3. Molecular formula: C22H32NP. Mole weight: 341.479g/mol. IUPAC Name: 2-(2-ditert-butylphosphanylphenyl)-N,N-dimethylaniline. Rotatable Bond Count: 5. Exact Mass: 341.227g/mol. SMILES: CC (C) (C)P (C1=CC=CC=C1C2=CC=CC=C2N (C)C)C (C) (C)C. InChI: InChI=1S/C22H32NP/c1-21(2,3)24(22(4,5)6)20-16-12-10-14-18(20)17-13-9-11-15-19(17)23(7)8/h9-16H,1-8H3. InChIKey: PHLPNEHPCYZBNZ-UHFFFAOYSA-N. H-Bond Acceptor: 1. Monoisotopic Mass: 341.227g/mol. | |
Tetrakis (triphenylphosphine)palladium, Pd : 9.2 wt.% Quick inquiry Where to buy Suppliers range | Our company can provide customers with rich supported precious metal catalyst products such as palladium series, platinum series, rhodium series and ruthenium series. Our catalysts not only have high catalytic efficiency, strong selectivity, and recyclability, but also can be used in organic reactions such as hydrogenation, dehydrogenation, amination, and cyclization. In addition, some products can also be used as raw materials for various precious metal compounds. The company has formed a series of proprietary and characteristic process technologies, and is currently undergoing process improvement and upgrading. In short, our catalytic products can be widely used in medicine, new chemical materials, pesticides, dyes and pigments, environmental protection, new energy, electronics, basic chemicals and other fields. Uses: ·For elimination reaction, reduction reaction and alkylation reaction; ·Make alkenyl chloride and alkyl lithium or Grignard reagent generate alkene and maintain configuration; ·Make alkenyl chloride and potassium cyanide generate alkenyl cyanide; ·Synthesis of ketones from acid chlorides; deodorization of brominated ketones with hydrogen; ·Preparation of alkynes and enones; ·Cyclization of rings in asymmetric biphenyls; ·Isomerization of diene epoxides, allyl acetate; ·Stereosynthesis of alkenes and 1,4-dienes; ·Dimerization of butadiene. Group: Colloidal Catalysts. CAS No. 14221-01-3. Molecular Weight: 1155.56 g/mol. SMILES: [Pd]. c1ccc (cc1)P (c2ccccc2)c3ccccc3. c4ccc (cc4)P (c5ccccc5)c6ccccc6. c7ccc (cc7)P (c8ccccc8)c9ccccc9. c%10ccc (cc%10)P (c%11ccccc%11)c%12ccccc%12. InChI: NFHFRUOZVGFOOS-UHFFFAOYSA-N. Boiling Point: 103-107 °C. Flash Point: 99 %. Density: Soluble in benzene, toluene, insoluble in ether and alcohol. | |
Tris (acetonitrile) cyclopentadienylruthenium (II) Hexafluorophosphate Quick inquiry Where to buy Suppliers range | yellow to orange powder. Uses: Catalyst used for the coupling of allene with activated olefines to form 1,3-diene. Catalyst used for the dimerization of propargyl alcohols. Catalyst used in the Trost's ruthenium-catalyzed ene-yne cross-coupling reaction. Catalyst for asymmetric cyclization of ω-hydroxy allyl alcohols to give α-alkenyl cyclic ethers. Catalyst for synthesis of furans from bis(alkynes) and DMSO. Group: Ruthenium series catalysts. Alternative Names: (Cyclopentadienyltris (acetonitrile)ruthenium hexafluorophosphate. Grades: 0.98. CAS No. 80049-61-2. Molecular formula: C11H14F6N3PRu. Mole weight: 434.29. Symbol: GHS07. Safty Description: Warning. Hazard statements: H315-H319-H335. | |
Tris(triphenylphosphine)rhodium(I) Chloride Quick inquiry Where to buy Suppliers range | Tris(triphenylphosphine)rhodium(I) Chloride. Uses: A homogeneous hydrogenation catalyst which operates under mild conditions. Catalyst for the decarbonylation of aldehydes. Catalyst for regio- and stereoselective allylic substitution reactions. Alkyne hydro-phosphorylation Heck-type reaction with α,β-unsaturated esters. Alkyne arylation Allylic alcohol-olefin coupling. Terminal alkenes from ketones. Rh-catalyzed isomerization of α-aryl propargyl alcohols to indanones. Reductive deprotection of silyl groups. Group: Rhodium series of catalysts. Alternative Names: Wilkinson's catalyst Tris(triphenylphosphine)rhodium(I) chloride C54H45ClP3Rh 925.23 ca 250 degrees dec. 14694-95-2 "14,10047" 238-744-5 MFCD00010016 P273-P501a; Tris(triphenylphosphine)rhodium chloride; AS-12487; AN-15374; Tris(triphenylphosphine)rhodium monochloride; 16592-65-7; RhCl(PPh3)3, Rhodium(I) tris(triphenylphosphine) chloride, Wilkinson's catalyst, NSC 124140; chlorotris(triphenylphosphine)-rhodium(i); RTR-005847; tris(triphenylphosphine)-rhodium (I) chloride. CAS No. 14694-95-2. Molecular formula: C54H45ClP3Rh-. Mole weight: 925.231g/mol. IUPAC Name: rhodium;triphenylphosphane;chloride. Rotatable Bond Count: 9. Exact Mass: 924.148g/mol. EC Number: 238-744-5. SMILES: 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-]. [Rh]. InChI: InChI=1S/3C18H15P.ClH.Rh/c3*1-4-10-16(11-5-1)19(17-12-6-2-7-13-17)18-14-8-3-9-15-18;;/h3*1-15H;1H;/p-1. InChIKey: QBERHIJABFXGRZ-UHFFFAOYSA-M. H-Bond Acceptor: 1. Monoisotopic Mass: 924.148g/mol. | |
Vanadium(III) chloride tetrahydrofuran complex (1:3) Quick inquiry Where to buy Suppliers range | Vanadium(III) chloride tetrahydrofuran complex (1:3). Uses: Catalyst used for oxidation of a wide variety allylic alcohols. Group: Metal & Ceramic Materials. Alternative Names: Trichlorotris (tetrahydrofuran)vanadium; 19559-06-9; Vanadium (III) chloride-tetrahydrofuran complex (1:3), 0.5M solution in methylene chloride, AcroSeal(R); MFCD00145515; SCHEMBL7929736; Vanadium(III) chloride tetrahydrofuran adduct;Vanadium(III) chloride tetrahydrofuran complex (1:3), 97%. CAS No. 19559-06-9. Molecular formula: C4H8Cl3OV. Mole weight: 229.398g/mol. IUPAC Name: oxolane;trichlorovanadium. Exact Mass: 227.908g/mol. SMILES: C1CCOC1.Cl[V](Cl)Cl. InChI: InChI=1S/C4H8O.3ClH.V/c1-2-4-5-3-1;;;;/h1-4H2;3*1H;/q;;;;+3/p-3. InChIKey: WARDLUZTYLPMGJ-UHFFFAOYSA-K. H-Bond Acceptor: 1. Monoisotopic Mass: 227.908g/mol. | |
Vanadyl(II) ethyl/butyl phosphonate Silica (PhosphonicS POVO) Quick inquiry Where to buy Suppliers range | Vanadyl(II) ethyl/butyl phosphonate Silica (PhosphonicS POVO). Uses: Catalyst used for oxidation of a wide variety allylic alcohols. |