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| Product | Description | |
|---|---|---|
| aryl-alcohol dehydrogenase | A group of enzymes with broad specificity towards primary alcohols with an aromatic or cyclohex-1-ene ring, but with low or no activity towards short-chain aliphatic alcohols. Group: Enzymes. Synonyms: p-hydroxybenzyl alcohol dehydrogenase; benzyl alcohol dehydrogenase; coniferyl alcohol dehydrogenase. Enzyme Commission Number: EC 1.1.1.90. CAS No. 37250-26-3. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-0374; aryl-alcohol dehydrogenase; EC 1.1.1.90; 37250-26-3; p-hydroxybenzyl alcohol dehydrogenase; benzyl alcohol dehydrogenase; coniferyl alcohol dehydrogenase. Cat No: EXWM-0374. |  |
| aryl-alcohol dehydrogenase (NADP+) | Also acts on some aliphatic aldehydes, but cinnamaldehyde was the best substrate found. Group: Enzymes. Synonyms: aryl alcohol dehydrogenase (nicotinamide adenine dinucleotide phosphate); coniferyl alcohol dehydrogenase; NADPH-linked benzaldehyde reductase; aryl-alcohol dehydrogenase (NADP). Enzyme Commission Number: EC 1.1.1.91. CAS No. 37250-27-4. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-0375; aryl-alcohol dehydrogenase (NADP+); EC 1.1.1.91; 37250-27-4; aryl alcohol dehydrogenase (nicotinamide adenine dinucleotide phosphate); coniferyl alcohol dehydrogenase; NADPH-linked benzaldehyde reductase; aryl-alcohol dehydrogenase (NADP). Cat No: EXWM-0375. | |
| aryl-alcohol oxidase | Oxidizes many primary alcohols containing an aromatic ring; best substrates are (2-naphthyl)methanol and 3-methoxybenzyl alcohol. Group: Enzymes. Synonyms: aryl alcohol oxidase; veratryl alcohol oxidase; arom. alcohol oxidase. Enzyme Commission Number: EC 1.1.3.7. CAS No. 9028-77-7. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-0425; aryl-alcohol oxidase; EC 1.1.3.7; 9028-77-7; aryl alcohol oxidase; veratryl alcohol oxidase; arom. alcohol oxidase. Cat No: EXWM-0425. | |
| 1,10-Phenanthroline Nickel dibromide | 1,10-Phenanthroline Nickel dibromide is a Ni precatalyst used for a variety of cross-coupling reactions, including N-alkylation of amides and arylation of alcohols. Uses: Transition metal catalysts. Synonyms: Nickel, dibromo(1,10-phenanthroline-κN1,κN10)-; Dibromo(1,10-phenanthroline-κN1,κN10)nickel; Nickel, dibromo(1,10-phenanthroline)-; Nickel, dibromo(1,10-phenanthroline-N1,N10)-; Dibromo(1,10-phenanthroline-κN1,κN10)nickel; 1,10-Phenanthroline nickel (II) dibromide; Ni (phen) Br2; (phen)NiBr2. Grades: ≥95%. CAS No. 48165-50-0. Molecular formula: C12H8Br2N2Ni. Mole weight: 398.71. |  |
| 1,1'-Bis(dicyclohexylphosphino)ferrocene | 1,1'-Bis(dicyclohexylphosphino)ferrocene. Uses: Ligand for palladium-catalyzed synthesis of oxindoles by amide ?-arylation. ligand for palladium-catalyzed alkoxycarbonylation of aryl chlorides. ligand for ruthenium-catalyzed alcohol-allene c-c coupling reaction via hydrohydroxyalkylation of 1,1-disubstituted allenes employing alcohols. ligand for nickel-catalyzed cross-coupling reaction of arylboronic acids with aryl carbonates. ligand for palladium-catalyzed regiodivergent hydroesterification of aryl olefins with phenyl formate to form linear structured phenyl arylpropanoates. ligand for palladium-catalyzed direct borylation of benzyl alcohol and its analogues in the absence of bases. Additional or Alternative Names: 1,1-Bis(dicyclohexylphosphino)ferrocene; 1,1-Bis(Dicyclohexylphosphino)Ferrocene; 1,1-BIS(DICYCLOHEXYLPHOSPHINO)FERROCENE. Product Category: Organic Phosphine Compounds. Appearance: Orange-red powder. CAS No. 146960-90-9. Molecular formula: C34H52FeP2. Mole weight: 578.57. Purity: 0.98. IUPACName: dicyclohexyl(cyclopentyl)phosphane;iron. Canonical SMILES: C1CCC(CC1)P(C2CCCCC2)[C]3[CH][CH][CH][CH]3.C1CCC(CC1)P(C2CCCCC2)[C]3[CH][CH][CH][CH]3.[Fe]. Product ID: ACM146960909. Alfa Chemistry ISO 9001:2015 Certified. Categories: AKOS026674396. |  |
| 1,1'-Bis(diisopropylphosphino)ferrocene | 1,1'-Bis(diisopropylphosphino)ferrocene. 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. Additional or Alternative Names: 1,1-BIS(DIISOPROPYLPHOSPHINO)FERROCENE. Product Category: Organic Phosphine Compounds. Appearance: Orange-yellow powder. CAS No. 97239-80-0. Molecular formula: C22H36FeP2. Mole weight: 418.32. Purity: 0.98. IUPACName: 1,1-Bis(diisopropylphosphino)ferrocene. Product ID: ACM97239800. Alfa Chemistry ISO 9001:2015 Certified. Categories: 1,1\'-Bis(diisopropylphosphino)ferrocene. | |
| 1,1-Dimethylethyl Nitrite | ert-Butyl nitrite is an intermediate used for diazotization and nitrosation of alcohols, thiols, amines and cycloalkanes. It is also used to prepare aryl azides from aryl amines. Group: Biochemicals. Grades: Highly Purified. CAS No. 540-80-7. Pack Sizes: 1g, 10g. Molecular Formula: C4H9NO2. US Biological Life Sciences. |  Worldwide |
| 1-(3-Methoxyphenyl)ethanol | 1-(3-Methoxyphenyl)ethanol (Rivastigmine EP Impurity G) is a versatile reactant used in the preparation of 2,3-dihydroimidazo[1,2-a]pyridines as enantioselective acyl transfer catalysts in kinetic resolution of alcohols. Also used in chemoselective preparation of aryl aldehydes/ketones via in situ generated TEMPO-copper(II) diimine catalyzed oxidation of benzylic alcohols in aqueous media. Group: Biochemicals. Grades: Highly Purified. CAS No. 23308-82-9. Pack Sizes: 50mg, 250mg. Molecular Formula: C9H12O2. US Biological Life Sciences. | Worldwide |
| (1R,3R,4R)-(-)-3,5-Dinitrobenzoate Menthol | (1S,3S,4S)-(-)-3,5-dinitrobenzoate Menthol is an intermediate in the synthesis of (±)-Neoisomenthol (N389960) which is a useful synthetic intermediate. It is used to prepare alkyl and aryl esters by chemoselective acylation of alkyl and aryl alcohols with carboxylic acid anhydrides in the presence of magnesium bis (trifluoro methyl sulfonyl) amide under solvent-free conditions. Group: Biochemicals. Grades: Highly Purified. CAS No. 1195710-85-0. Pack Sizes: 50mg, 100mg. Molecular Formula: C17H22N2O6. US Biological Life Sciences. | Worldwide |
| (1S)-1-Amino-2-methyl-1-phenylpropan-2-ol | (1S)-1-Amino-2-methyl-1-phenylpropan-2-ol can be used as reactant/reagent in stereoselective preparation of diaryl carbonyl compounds via palladium-catalyzed enantioselective redox-relay oxidative Heck arylation of arylboronic acids and homoallylic alcohols. Group: Biochemicals. Grades: Highly Purified. CAS No. 110480-86-9. Pack Sizes: 100mg, 250mg. Molecular Formula: C10H15NO, Molecular Weight: 165.23. 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. | |
| 2,3-Difluorobenzyl alcohol | 2,3-Difluorobenzyl alcohol. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Benzenemethanol, 2,3-difluoro-. Product Category: Aryl Fluorinated Building Blocks. CAS No. 75853-18-8. Molecular formula: C7H6F2O. Mole weight: 144.12. Purity: 98%+. IUPACName: (2,3-difluorophenyl)methanol. Canonical SMILES: C1=CC(=C(C(=C1)F)F)CO. Density: 1.282 g/ml. Product ID: ACM75853188. Alfa Chemistry ISO 9001:2015 Certified. | |
| 2,4-Dimethoxybenzyl alcohol | 2,4-Dimethoxybenzyl alcohol, an aromatic alcohol, is a substrate of glucose-methanol-choline (GMC) oxidoreductase. GMC oxidoreductase displays the characteristics of an aryl-alcohol oxidase [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 7314-44-5. Pack Sizes: 10 mM * 1 mL; 5 g; 10 g; 25 g. Product ID: HY-W007584. |  |
| 2-Chloro-5-(trifluoromethyl)benzyl alcohol | 2-Chloro-5-(trifluoromethyl)benzyl alcohol. Uses: Designed for use in research and industrial production. Product Category: Aryl. CAS No. 64372-62-9. Molecular formula: C7H8ClNO. Mole weight: 210.58. Product ID: ACM64372629. Alfa Chemistry ISO 9001:2015 Certified. Categories: 2-Chloro-5-(trifluoromethyl)benzylalcohol. | |
| 2-(Dibutylamino)-1-(2,7-dichloro-9H-fluoren-4-yl)ethanol | 2-(Dibutylamino)-1-(2,7-dichloror-9H-fluoren-4-yl)ethanol is an impurity formed during the synthesis of Lumefantrine, a fluorene derivative belonging to the aryl amino alcohol class of anti-malarial drugs. Synonyms: 2,7-Dichloro-α-[(dibutylamino)methyl]-9H-fluorene-4-methanol. Grades: > 95%. CAS No. 69759-61-1. Molecular formula: C23H29Cl2NO. Mole weight: 406.39. | |
| 2-(Dibutylamino)-1-(2,7-dichloro-9H-fluoren-4-yl)ethanol | 2-(Dibutylamino)-1-(2,7-dichloror-9H-fluoren-4-yl)ethanol is an impurity formed during the synthesis of Lumefantrine (L474000), a fluorene (F462000) derivative belonging to the aryl amino alcohol class of anti-malarial drugs. Group: Biochemicals. Alternative Names: 2,7-Dichloro-α-[(dibutylamino)methyl]-9H-fluorene-4-methanol. Grades: Highly Purified. CAS No. 69759-61-1. Pack Sizes: 1g. US Biological Life Sciences. | Worldwide |
| 2-(Dicyclohexylphosphino)biphenyl | 2-(Dicyclohexylphosphino)biphenyl. Uses: Ligand used in the palladium-catalyzed synthesis of aromatic amines from aryl chlorides, bromides and triflates. ligand employed in suzuki coupling reactions involving aryl chlorides, bromides and triflates. useful ligand for the pd-catalyzed oxidation of alcohols in the presence of chlorobenzenes. useful ligand for the pd-catalyzed amination with ammonia equivalents. ligand for the gold(I)-catalyzed intramolecular [4+2] cycloadditions involving 1,3-enynes and arylalkynes with alkenes. ligand used in the palladium-catalyzed borylation of aryl bromdies. ligand used in the palladium-catalyzed siliylation of aryl chlorides. Additional or Alternative Names: Cyclohexyl JohnPhos. Product Category: Organic Phosphine Compounds. Appearance: Solid. CAS No. 247940-06-3. Molecular formula: C24H31P. Mole weight: 350.48. Purity: 0.98. IUPACName: dicyclohexyl-(2-phenylphenyl)phosphane. Canonical SMILES: C1CCC(CC1)P(C2CCCCC2)C3=CC=CC=C3C4=CC=CC=C4. ECNumber: 480-030-2. Product ID: ACM247940063-1. Alfa Chemistry ISO 9001:2015 Certified. | |
| 2-Fluoro-5-nitrobenzyl alcohol | 2-Fluoro-5-nitrobenzyl alcohol. Uses: Designed for use in research and industrial production. Product Category: Aryl Fluorinated Building Blocks. CAS No. 63878-73-9. Molecular formula: C7H6ClFS. Mole weight: 171.13. Product ID: ACM63878739-1. Alfa Chemistry ISO 9001:2015 Certified. Categories: (2-fluoro-5-nitrophenyl)methanol. | |
| 2-Methyl-2-hexanol | 2-Methyl-2-hexanol. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Butyldimethylcarbinol, tert-Heptanol, 2-METHYL-2-HEXANOL, 2-Hexanol, 2-methyl-, 2-Methylhexan-2-ol, tert-HEPTYL ALCOHOL, tert-Heptanol (9CI), 111600_ALDRICH, NSC21977, CID12240, EINECS 210-881-5, NSC 21977, ZINC01589668, 2-Hexanol, 2-methyl- (8CI)(9CI), LS-74712, TL8004169, 625-23-0, 28929-86-4. Product Category: Aryl. Appearance: CLEAR COLOURLESS TO LIGHT YELLOW LIQUID. CAS No. 625-23-0. Molecular formula: C7H16O. Mole weight: 116.2. Purity: 0.96. IUPACName: 2-methylhexan-2-ol. Canonical SMILES: CCCCC(C)(C)O. Density: 0.812 g/mL at 25ºC(lit.). ECNumber: 210-881-5. Product ID: ACM625230. Alfa Chemistry ISO 9001:2015 Certified. | |
| 2-(Trifluoromethyl)benzyl alcohol | 2-(Trifluoromethyl)benzyl alcohol. Uses: Designed for use in research and industrial production. Product Category: Aryl. CAS No. 346-06-5. Molecular formula: C13H11Br. Mole weight: 176.14. Product ID: ACM346065. Alfa Chemistry ISO 9001:2015 Certified. | |
| 3,4,7,8-Tetramethyl-1,10-phenanthroline Nickel (II) dichloride | 3,4,7,8-Tetramethyl-1,10-phenanthroline Nickel (II) dichloride is a Ni catalyst used for a variety of cross-coupling reactions including the cross-electrophile coupling of benzyl alcohols and aryl halides. Uses: Transition metal catalysts. Synonyms: Nickel, dichloro(3,4,7,8-tetramethyl-1,10-phenanthroline-κN1,κN10)-; Dichloro(3,4,7,8-tetramethyl-1,10-phenanthroline-κN1,κN10)nickel; (Me4Phen)NiCl2. Grades: ≥95%. CAS No. 2254430-88-9. Molecular formula: C16H16Cl2N2Ni. Mole weight: 365.91. | |
| 3,4-Difluorobenzyl alcohol | 3,4-Difluorobenzyl alcohol. Uses: Designed for use in research and industrial production. Product Category: Aryl Fluorinated Building Blocks. CAS No. 85118-05-4. Mole weight: 144.12. Product ID: ACM85118054. Alfa Chemistry ISO 9001:2015 Certified. | |
| 3-Bromo-5-hydroxybenzyl Alcohol | 3-Bromo-5-hydroxybenzyl Alcohol is an intermediate used to prepare (isoxazolylphenyl) arylmethanols as inhibitors of the BET bromodomain family member BRD4(1) for potential use as antitumor agents. Group: Biochemicals. Grades: Highly Purified. CAS No. 1020336-51-9. Pack Sizes: 500mg, 1g. Molecular Formula: C7H7BrO2, Molecular Weight: 203.03. US Biological Life Sciences. | Worldwide |
| 3-Fluoro-4-(hydroxymethyl)benzonitrile | 3-Fluoro-4-(hydroxymethyl)benzonitrile. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Benzonitrile, 3-fluoro-4-(hydroxymethyl)- (9CI);3-Fluoro-4-(hydroxymethyl)benzonitrile;4-Cyano-2-fluorobenzyl alcohol. Product Category: Aryl Fluorinated Building Blocks. CAS No. 219873-06-0. Molecular formula: C8H6FNO. Mole weight: 151.14. Purity: 0.96. IUPACName: 3-fluoro-4-(hydroxymethyl)benzonitrile. Canonical SMILES: C1=CC(=C(C=C1C#N)F)CO. Density: 1.27g/cm³. Product ID: ACM219873060. Alfa Chemistry ISO 9001:2015 Certified. Categories: 3-Fluoro-4-hydroxymethylbenzonitrile. | |
| 3-(Hydroxymethyl)phenylboronic acid | Reactant involved in: Copper-mediated trifluoromethylation Copper-catalyzed transformations from arylboronic acids in water Mitsunobu, Suzuki, and amidation reactions with hydroxyphenylamino bromopyrazinecarboxylateReactant involved in the synthesis of biologically active molecules including: Mycobacterium tuberculosis H37Rv chorismate mutase inhibitors via Suzuki coupling reactions HIV protease inhibitors with antiviral activity against drug-resistant viruses Pyrrole derivatives for use as PDE4B inhibitors. Synonyms: 3-Boronobenzyl alcohol; 3-hydroxymethylbenzeneboronic acid; 3-hydroxymethylboronic acid; RARECHEM AH PB 0189; 3-HydroMethylphenylboronicacid; KS-000000LJ; m-(Hydroxymethyl)phenyl boronic acid. Grades: 97%. CAS No. 87199-15-3. Molecular formula: C7H9BO3. Mole weight: 151.96. | |
| 4-Fluoro-3-nitrobenzyl alcohol | 4-Fluoro-3-nitrobenzyl alcohol. Uses: Designed for use in research and industrial production. Product Category: Aryl Fluorinated Building Blocks. CAS No. 20274-69-5. Molecular formula: C7H6ClFO3S. Mole weight: 171.13. Product ID: ACM20274695. Alfa Chemistry ISO 9001:2015 Certified. | |
| 4-Fluoro-α-methylbenzyl alcohol | 4-Fluoro-α-methylbenzyl alcohol. Uses: Designed for use in research and industrial production. Product Category: Aryl Fluorinated Building Blocks. CAS No. 403-41-8. Mole weight: 140.15. Product ID: ACM403418. Alfa Chemistry ISO 9001:2015 Certified. | |
| 4-Iodobenzyl alcohol | 4-Iodobenzyl alcohol. Uses: Designed for use in research and industrial production. Product Category: Aryl. CAS No. 18282-51-4. Mole weight: 234.03. Product ID: ACM18282514. Alfa Chemistry ISO 9001:2015 Certified. | |
| 4-Isopropylbenzyl Alcohol | 4-Isopropylbenzyl Alcohol. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 4-(1-Methylethyl)benzenemethanol. Product Category: Aryl. Appearance: Colorless to pale yellow clear liquid. CAS No. 536-60-7. Molecular formula: C10H14O. Mole weight: 150.22. Purity: 95%+. IUPACName: (4-Propan-2-ylphenyl)methanol. Canonical SMILES: CC(C)C1=CC=C(C=C1)CO. Density: 0.982 g/mL at 25 °C(lit.). ECNumber: 208-640-4. Product ID: ACM536607. Alfa Chemistry ISO 9001:2015 Certified. | |
| 5-Fluoro-2-mercaptobenzyl alcohol | 5-Fluoro-2-mercaptobenzyl alcohol. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 639249_ALDRICH, 5-Fluoro-2-mercaptophenylmethanol, MolPort-003-938-068, 5-Fluoro-2-mercaptobenzyl alcohol, (5-fluoro-2-mercaptophenyl)methanol, EN001026, 870703-84-7. Product Category: Aryl Fluorinated Building Blocks. CAS No. 870703-84-7. Molecular formula: C6H4ClF2N. Mole weight: 158.19. Purity: 0.96. IUPACName: (5-fluoro-2-sulfanylphenyl)methanol. Canonical SMILES: C1=CC(=C(C=C1F)CO)S. Product ID: ACM870703847. Alfa Chemistry ISO 9001:2015 Certified. | |
| 5-(hydroxymethyl)furfural oxidase | The enzyme, characterized from the bacterium Methylovorus sp. strain MP688, is involved in the degradation and detoxification of 5-(hydroxymethyl)furfural. The enzyme acts only on alcohol groups and requires the spontaneous hydration of aldehyde groups for their oxidation. The enzyme has a broad substrate range that overlaps with EC 1.1.3.7, aryl-alcohol oxidase. Group: Enzymes. Enzyme Commission Number: EC 1.1.3.47. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-0420; 5-(hydroxymethyl)furfural oxidase; EC 1.1.3.47. Cat No: EXWM-0420. | |
| 5-Methyl-1-hexanol | Iso heptyl alcohol appears as a clear colorless liquid with a pleasant odor. Less dense than water and insoluble in water. Vapors heavier than air. Used to make other chemicals, as a solvent, and in cosmetic formulations. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 5-Methylhexan-1-ol;5-METHYL-1-HEXANOL;627-98-5;5-methylhexanol;Isoheptanol;Isoheptan-1-ol;1-Hexanol, 5-methyl-;51774-11-9;5-Methyl-hexan-1-ol;UNII-1PLY0QE25K;1PLY0QE25K;UNII-Q766MX3689;MFCD00072703;Q766MX3689;EINECS 257-413-6;isoheptyl alcohol;EINECS 211-023-2;5-Methylhexanol-[d7];ACMC-1AXQ8;Isoheptanol (mixed isomers);5-Methyl-1-hexanol, 97%;SCHEMBL104527;DTXSID4075326;ZINC2031628;GEO-01853;AKOS009156368;FS-5402;SY083602;BB 0258104;FT-0671815;FT-0671816;R1957;W-109236. Product Category: Aryl. CAS No. 627-98-5. Molecular formula: C7H16O;C7H16O. Mole weight: 116.20g/mol. IUPACName: 5-methylhexan-1-ol. Canonical SMILES: CC(C)CCCCO. ECNumber: 211-023-2;257-413-6. Product ID: ACM627985. Alfa Chemistry ISO 9001:2015 Certified. | |
| ABC294640 | ABC294640 is an orally available, aryladamantane compound and selective inhibitor of sphingosine kinase-2 (SK2) with potential antineoplastic activity. Upon administration, ABC294640 competitively binds to and inhibits SK2, thereby preventing the phosphorylation of the pro-apoptotic amino alcohol sphingosine to sphingosine 1-phosphate (S1P), the lipid mediator that is pro-survival and critical for immunomodulation. Synonyms: ABC-294640; ABC294640; ABC 294640; Opaganib; 3-(4-chlorophenyl)-adamantane-1-carboxylic acid (pyridin-4-ylmethyl)amide. Grades: 0.98. CAS No. 915385-81-8. Molecular formula: C23H25ClN2O. Mole weight: 380.9104. | |
| acetylsalicylate deacetylase | Not identical with EC 3.1.1.1 (carboxylesterase), EC 3.1.1.2 (arylesterase), EC 3.1.1.7 (acetylcholinesterase) or EC 3.1.1.8 (cholinesterase). The activity of the liver cytosol enzyme is highest with acetyl esters of aryl alcohols, and thioesters are also hydrolysed; the microsomal enzyme also hydrolyses some other negatively charged esters, with highest activity on esters of salicylate with long-chain alcohols. Group: Enzymes. Synonyms: aspirin esterase; aspirin esterase; acetylsalicylic acid esterase; aspirin hydrolase. Enzyme Commission Number: EC 3.1.1.55. CAS No. 87348-04-7. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-3483; acetylsalicylate deacetylase; EC 3.1.1.55; 87348-04-7; aspirin esterase; aspirin esterase; acetylsalicylic acid esterase; aspirin hydrolase. Cat No: EXWM-3483. | |
| Allyl[1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene]chloropalladium(II) | Allyl[1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene]chloropalladium(II). 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. Additional or 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)?-. Product Category: Organic Phosphine Compounds. Appearance: white solid. CAS No. 478980-03-9. Molecular formula: C30H42ClN2Pd. Mole weight: 572.54. Purity: 98%, Pd>18.5%. Product ID: ACM478980039. Alfa Chemistry ISO 9001:2015 Certified. | |
| (±)-α-(Trifluoromethyl)benzyl alcohol | (±)-α-(Trifluoromethyl)benzyl alcohol. Uses: Designed for use in research and industrial production. Product Category: Aryl. CAS No. 340-05-6. Molecular formula: C7F7I. Mole weight: 176.14. Product ID: ACM340056. Alfa Chemistry ISO 9001:2015 Certified. | |
| 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. | |
| Chrysanthemyl alcohol,mixture of cis and trans | Chrysanthemyl alcohol,mixture of cis and trans. Uses: Designed for use in research and industrial production. Product Category: Aryl. CAS No. 5617-92-5. Molecular formula: C6H7FN2. Mole weight: 154.25. Product ID: ACM5617925. Alfa Chemistry ISO 9001:2015 Certified. | |
| coniferin β-glucosidase | Also hydrolyses syringin, 4-cinnamyl alcohol β-glucoside and, more slowly, some other aryl β-glycosides. A plant cell-wall enzyme involved in the biosynthesis of lignin. Group: Enzymes. Synonyms: coniferin-hydrolyzing β-glucosidase. Enzyme Commission Number: EC 3.2.1.126. CAS No. 83869-30-1. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-3809; coniferin β-glucosidase; EC 3.2.1.126; 83869-30-1; coniferin-hydrolyzing β-glucosidase. Cat No: EXWM-3809. | |
| Dimethylbenzylcarbinol | Dimethylbenzylcarbinol. Uses: Designed for use in research and industrial production. Additional or Alternative Names: AKOS009156717; Dimethylbenzylcarbinol; NSC27228; FEMA No. 2393; MFCD00004465; alpha,alpha-dimethylphenylethyl alcohol; DTXSID1047601; 2-Methyl-1-phenylpropan-2-ol; Phenethyl alcohol. alpha.. alpha.-dimethyl-; WLN: QX1 & 1 & 1R. Product Category: Aryl. CAS No. 100-86-7. Molecular formula: C10H14O. Mole weight: 150.221g/mol. IUPACName: 2-methyl-1-phenylpropan-2-ol. Canonical SMILES: CC(C)(CC1=CC=CC=C1)O. ECNumber: 202-896-0. Product ID: ACM100867. Alfa Chemistry ISO 9001:2015 Certified. Categories: 2-Methyl-1-phenyl-2-propanol. | |
| DL-Phenylglycinol | A chiral arylalkylamine used as organocatalysts. Used in the synthesis and chiral recognition properties of novel fluorescent chemosensors for amino acid. Group: Biochemicals. Alternative Names: β-Aminobenzeneethanol; β-Aminophenethyl Alcohol; (RS)-Phenylglycinol; (±)-2-Amino-2-phenylethanol; (±)-Phenylglycinol; 2-Amino-2-phenylethanol; 2-Hydroxy-1-phenylethylamine; 2-Phenyl-2-aminoethanol; DL-α-Phenylglycinol; Phenylglycinol; α - (Hydroxymethyl) benzylamine. Grades: Highly Purified. CAS No. 7568-92-5. Pack Sizes: 10g. US Biological Life Sciences. | Worldwide |
| Esterase from Bacillus subtilis, Recombinant | An esterase is a hydrolase that splits esters into acids and alcohols. Applications: Esterase, from bacillus subtilis, may be used in protein engineering research as well as to study the kinetic resolution of acetates of arylaliphatic tertiary alcohols. this product is recombinant and expressed in e. coli (> 10 units/mg). Group: Enzymes. Synonyms: EC 3.1.1.1; ali-esterase; B-esterase; monobutyrase; cocaine esterase; procaine esterase; methylbutyrase; vitamin A esterase; butyryl esterase; carboxyesterase; carboxylate esterase; carboxylic esterase; methylbutyrate esterase; triacet. Enzyme Commission Number: EC 3.1.1.1. CAS No. 9016-18-6. Esterase. Activity: Type I, > 10 units/mg; Type II, > 0.8 units/mg. Storage: -20°C. Source: E. coli. Species: Bacillus subtilis. EC 3.1.1.1; ali-esterase; B-esterase; monobutyrase; cocaine esterase; procaine esterase; methylbutyrase; vitamin A esterase; butyryl esterase; carboxyesterase; carboxylate esterase; carboxylic esterase; methylbutyrate esterase; triacetin esterase; carboxyl ester hydrolase; butyrate esterase; methylbutyrase; α-carboxylesterase; propionyl esterase; nonspecific carboxylesterase; esterase D; esterase B; esterase A; serine esterase; carboxylic acid esterase; cocaine esterase; 9016-18-6. Pack: Bottomless glass bottle. Contents are inside inserted fused cone. Cat No: NATE-0242. | |
| Ir[FCF3(CF3)ppy]2(dtbbpy)PF6 | Ir[FCF3(CF3)ppy]2(dtbbpy)PF6 is a versatile photocatalyst that can be used for a variety of synthetic transformations including the α-arylation of alcohols. Uses: Transition metal catalysts. Synonyms: Bis[2-(2-fluoro-4-(trifluoromethyl)phenyl)-5-(trifluoromethyl)pyridine][4,4'-di-tert-butyl-2,2'-bipyridine] iridium(III) hexafluorophosphate; Iridium(1+), [4,4'-bis(1,1-dimethylethyl)-2,2'-bipyridine-κN1,κN1']bis[3-fluoro-5-(trifluoromethyl)-2-[5-(trifluoromethyl)-2-pyridinyl-κN]phenyl-κC]-, (OC-6-33)-, hexafluorophosphate(1-) (1:1). Grades: ≥95%. CAS No. 2222402-20-0. Molecular formula: C44H34F14IrN4.F6P. Mole weight: 1221.93. | |
| Me4tButylXphos | Me4tButylXphos. Uses: Ligand for the palladium-catalyzed amidation of aryl chlorides. ligand for the palladium-catalyzed synthesis of phenols from aryl halides. ligand for the palladium-catalyzed coupling of aryl halides and secondary alcohols. Additional or Alternative Names: Di-tert-butyl[3,4,5,6-tetramethyl-2',4',6'-tri(propan-2-yl)[1,1'-biphenyl]-2-yl]phosphane; Di-tert-butyl(2',4',6'-triisopropyl-3,4,5,6-tetramethyl-[1,1'-biphenyl]-2-yl)phosphine; Tetramethyl Di-tbutyl X-Phos; MFCD09038436; 2-DI-TERT-BUTYLPHOSPHINO-3,4,5,6-TETRAMETHYL-2',4',6'-TRI ISOPROPYLIBIPHENYL; di-tert-butyl(2',4',6'-triisopropyl-3,4,5,6-tetramethyl-[1,1'-biphenyl]-2-yl)phosphane; 2-DI-TERT-BUTYLPHOSPHINO-3,4,5,6-TETRAM&; 2-(di-tert-butylphosphino)-2',4',6'-triisopropyl-3,4,5,6-tetramethyl-1,1'-biphenyl; CS-W001169; ZINC56961829. Product Category: Organic Phosphine Compounds. CAS No. 857356-94-6. Molecular formula: C33H53P. Mole weight: 480.761g/mol. IUPACName: ditert-butyl-[2,3,4,5-tetramethyl-6-[2,4,6-tri(propan-2-yl)phenyl]phenyl]phosphane. Canonical SMILES: CC1=C(C(=C(C(=C1C)C2=C(C=C(C=C2C(C)C)C(C)C)C(C)C)P(C(C)(C)C)C(C)(C)C)C)C. Product ID: ACM857356946. Alfa Chemistry ISO 9001:2015 Certified. Categories: di-tert-butyl[3,4,5,6-tetramethyl-2',4',6'-tris(propan-2-yl)-[1,1'-biphenyl]-2-yl]phosphane. | |
| Native Abalone Sulfatase | Sulfatases EC 3.1.6.1 are enzymes of the esterase class that catalyze the hydrolysis of sulfate esters. These may be found on a range of substrates, including steroids, carbohydrates and proteins. Sulfate esters may be formed from various alcohols and amines. In the latter case the resultant N-sulfates can also be termed sulfamates. Sulfatases play important roles in the cycling of sulfur in the environment, in the degradation of sulfated glycosaminoglycans and glycolipids in the lysosome, and in remodelling sulfated glycosaminoglycans in the extracellular space. Together with sulfotransferases, sulfatases form the major catalytic machinery for the synthesis and breakage of sulfa...ne conjugates from hamster embryo fibroblasts. Group: Enzymes. Synonyms: EC 3.1.6.1; 9016-17-5; sulfatase; nitrocatechol sulfatase; phenolsulfatase; phenylsulfatase; p-nitrophenyl sulfatase; arylsulfohydrolase; 4-methylumbelliferyl sulfatase; estrogen sulfatase; arylsulfatase. Enzyme Commission Number: EC 3.1.6.1. CAS No. 9016-17-5. Sulfatases. Activity: 20-40 units/mg solid. Storage: -20°C. Form: lyophilized powder. Source: Abalone entrails. Species: Abalone. EC 3.1.6.1; 9016-17-5; sulfatase; nitrocatechol sulfatase; phenolsulfatase; phenylsulfatase; p-nitrophenyl sulfatase; arylsulfohydrolase; 4-methylumbelliferyl sulfatase; estrogen sulfatase; arylsulfatase. Cat No: NATE-0685. | |
| Native Aerobacter aerogenes Sulfatase | Sulfatases EC 3.1.6.1 are enzymes of the esterase class that catalyze the hydrolysis of sulfate esters. These may be found on a range of substrates, including steroids, carbohydrates and proteins. Sulfate esters may be formed from various alcohols and amines. In the latter case the resultant N-sulfates can also be termed sulfamates. Sulfatases play important roles in the cycling of sulfur in the environment, in the degradation of sulfated glycosaminoglycans and glycolipids in the lysosome, and in remodelling sulfated glycosaminoglycans in the extracellular space. Together with sulfotransferases, sulfatases form the major catalytic machinery for the synthesis and breakage o...17-5; sulfatase; nitrocatechol sulfatase; phenolsulfatase; phenylsulfatase; p-nitrophenyl sulfatase; arylsulfohydrolase; 4-methylumbelliferyl sulfatase; estrogen sulfatase; arylsulfatase. Enzyme Commission Number: EC 3.1.6.1. CAS No. 9016-17-5. Sulfatases. Activity: 2-5 units/mg protein (biuret), 10-20 units/mL. Storage: -20°C. Form: buffered aqueous glycerol solution; Solution in 50% glycerol containing 0.01 M Tris, pH 7.5. Source: Aerobacter aerogenes. EC 3.1.6.1; 9016-17-5; sulfatase; nitrocatechol sulfatase; phenolsulfatase; phenylsulfatase; p-nitrophenyl sulfatase; arylsulfohydrolase; 4-methylumbelliferyl sulfatase; estrogen sulfatase; arylsulfatase. Cat No: NATE-0686. | |
| Native Helix pomatia Sulfatase | Sulfatases EC 3.1.6.1 are enzymes of the esterase class that catalyze the hydrolysis of sulfate esters. These may be found on a range of substrates, including steroids, carbohydrates and proteins. Sulfate esters may be formed from various alcohols and amines. In the latter case the resultant N-sulfates can also be termed sulfamates. Sulfatases play important roles in the cycling of sulfur in the environment, in the degradation of sulfated glycosaminoglycans and glycolipids in the lysosome, and in remodelling sulfated glycosaminoglycans in the extracellular space. Together with sulfotransferases, sulfatases form the major catalytic machinery for the synthesis and breakage of su...n. Group: Enzymes. Synonyms: EC 3.1.6.1; 9016-17-5; sulfatase; nitrocatechol sulfatase; phenolsulfatase; phenylsulfatase; p-nitrophenyl sulfatase; arylsulfohydrolase; 4-methylumbelliferyl sulfatase; estrogen sulfatase; arylsulfatase. Enzyme Commission Number: EC 3.1.6.1. CAS No. 9016-17-5. Sulfatases. Activity: Type I, > 10 ,000 units/g solid; Type II, > 2 ,000 units/mL. Storage: -20°C. Form: Type I, powder; Type II, aqueous solution. Source: Helix pomatia. EC 3.1.6.1; 9016-17-5; sulfatase; nitrocatechol sulfatase; phenolsulfatase; phenylsulfatase; p-nitrophenyl sulfatase; arylsulfohydrolase; 4-methylumbelliferyl sulfatase; estrogen sulfatase; arylsulfatase. Cat No: NATE-0687. | |
| Native Patella vulgata (keyhole limpet) Sulfatase | Sulfatases EC 3.1.6.1 are enzymes of the esterase class that catalyze the hydrolysis of sulfate esters. These may be found on a range of substrates, including steroids, carbohydrates and proteins. Sulfate esters may be formed from various alcohols and amines. In the latter case the resultant N-sulfates can also be termed sulfamates. Sulfatases play important roles in the cycling of sulfur in the environment, in the degradation of sulfated glycosaminoglycans and glycolipids in the lysosome, and in remodelling sulfated glycosaminoglycans in the extracellular space. Together with sulfotransferases, sulfatases form the major catalytic machinery for the synthesis and breakage of sulfate esters. Group: Enzymes. Synonyms: EC 3.1.6.1; 9016-17-5; sulfatase; nitrocatechol sulfatase; phenolsulfatase; phenylsulfatase; p-nitrophenyl sulfatase; arylsulfohydrolase; 4-methylumbellifery. Enzyme Commission Number: EC 3.1.6.1. CAS No. 9016-17-5. Sulfatases. Activity: Type I, > 10 units/mg solid; Type II, > 5 units/mg solid. Storage: -20°C. Form: essentially salt-free, lyophilized powder. Source: Patella vulgata (keyhole limpet). EC 3.1.6.1; 9016-17-5; sulfatase; nitrocatechol sulfatase; phenolsulfatase; phenylsulfatase; p-nitrophenyl sulfatase; arylsulfohydrolase; 4-methylumbelliferyl sulfatase; estrogen sulfatase; arylsulfatase. Cat No: NATE-0688. | |
| PhDave-Phos | PhDave-Phos. Uses: Useful ligand for sterically hindered substrates in the pd-catalyzed amination reactions of aryl bromides. ligand used for the cu-catalyzed phosphorylation of alcohols. ligand for pd-catalyzed c-h benzylation. ligand for palladium-catalyzed [4 + 2] benzannulation reaction. Additional or Alternative Names: SY030636; 2'-(DIPHENYLPHOSPHINO)-N,N-DIMETHYLBIPHENYL-2-AMINE; 2-Dimethylamino-2'-(diphenylphosphino)biphenyl; RL02764; AKOS015840665; 2-(Diphenylphosphino)-2 inverted exclamation mark -(N,N-dimethylamino)biphenyl; 2'-(DIPHENYLPHOSPHINO)-N,N'-DIMETHYL-(1,1'-BIPHENYL)-2-AMINE; 2'-(diphenylphosphanyl)-N,N-dimethyl-[1,1'-biphenyl]-2-amine; 2-DIPHENYLPHOSPHINO-2'-DIMETHYLAMINOBIPHENYL; AN-11455. Product Category: Organic Phosphine Compounds. CAS No. 240417-00-9. Molecular formula: C26H24NP. Mole weight: 381.459g/mol. IUPACName: 2-(2-diphenylphosphanylphenyl)-N,N-dimethylaniline. Canonical SMILES: CN(C)C1=CC=CC=C1C2=CC=CC=C2P(C3=CC=CC=C3)C4=CC=CC=C4. Product ID: ACM240417009. Alfa Chemistry ISO 9001:2015 Certified. Categories: 2-(DIPHENYLPHOSPHINO)-2'-(N,N-DIMETHYLAMINO)BIPHENYL. | |
| (R)-4-Fluoro-α-methylbenzyl alcohol | (R)-4-Fluoro-α-methylbenzyl alcohol. Uses: Designed for use in research and industrial production. Product Category: Aryl Fluorinated Building Blocks. CAS No. 101219-68-5. Mole weight: 140.15. Product ID: ACM101219685. Alfa Chemistry ISO 9001:2015 Certified. | |
| Rhodium(II) acetate dimer | 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: Salt electrolytessolution deposition precursors. Alternative Names: Tetrakis-(mu-acetato)dirhodium. CAS No. 15956-28-2. Product ID: rhodium(2+); tetraacetate. Molecular formula: 441.99. Mole weight: C8H12O8Rh2. CC(=O)[O-]. CC(=O)[O-]. CC(=O)[O-]. CC(=O)[O-]. [Rh+2]. [Rh+2]. InChI=1S/4C2H4O2.2Rh/c4*1-2(3)4; /h4*1H3, (H, 3, 4); /q; 2*+2/p-4. SYBXSZMNKDOUCA-UHFFFAOYSA-J. 98%. |  |
| RockPhos | RockPhos. Uses: Ligand used in the palladium-catalyzed c-o bond forming reactions of secondary and primary alcohols with a range of aryl halides. heterocyclic halides and, for the first time, electron-rich aryl halides can be coupled with secondary alcohols. Additional or Alternative Names: ZINC95910984; 2-(Di-t-butylphosphino)-3-methoxy-6-methyl-2'-4'-6'-tri-i-propyl-1,1'-biphenyl; RockPhos, 97%; di-tert-butyl-[6-methoxy-3-methyl-2-(2,4,6-triisopropylphenyl)phenyl]phosphane; Y-200021; Di-tert-butyl(2 inverted exclamation marka,4 inverted exclamation marka,6 inverted exclamation marka-triisopropyl-3-methoxy-6-methyl-[1,1 inverted exclamation marka-biphenyl]-2-yl)phosphine; CVLLAKCGAFNZHJ-UHFFFAOYSA-N; 2-Di-tert-butylphosphino-3-Methoxy-6-Methyl-2',4',6'-triisopropyl-1,1'-biphenyl; SCHEMBL12929986; AX8242285. Product Category: Organic Phosphine Compounds. CAS No. 1262046-34-3. Molecular formula: C31H49OP. Mole weight: 468.706g/mol. IUPACName: ditert-butyl-[6-methoxy-3-methyl-2-[2,4,6-tri(propan-2-yl)phenyl]phenyl]phosphane. Canonical SMILES: CC1=C(C(=C(C=C1)OC)P(C(C)(C)C)C(C)(C)C)C2=C(C=C(C=C2C(C)C)C(C)C)C(C)C. Product ID: ACM1262046343. Alfa Chemistry ISO 9001:2015 Certified. Categories: Rock phosphate. | |
| (S)-4-Fluoro-α-methylbenzyl alcohol | (S)-4-Fluoro-α-methylbenzyl alcohol. Uses: Designed for use in research and industrial production. Product Category: Aryl Fluorinated Building Blocks. CAS No. 101219-73-2. Molecular formula: C8H7BrF2. Mole weight: 140.15. Product ID: ACM101219732. Alfa Chemistry ISO 9001:2015 Certified. | |
| Silver trifluoromethanesulfonate | 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. Additional or 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. Product Category: Silver series of catalysts. Appearance: Powder. CAS No. 2923-28-6. Molecular formula: CAgF3O3S. Mole weight: 256.94. Purity: 0.98. IUPACName: silver;trifluoromethanesulfonate. Canonical SMILES: C(F)(F)(F)S(=O)(=O)[O-].[Ag+]. ECNumber: 220-882-2. Product ID: ACM2923286-1. Alfa Chemistry ISO 9001:2015 Certified. | |
| t-BuDavePhos | 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. Additional or 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. Product Category: Organic Phosphine Compounds. CAS No. 224311-49-3. Molecular formula: C22H32NP. Mole weight: 341.479g/mol. IUPACName: 2-(2-ditert-butylphosphanylphenyl)-N,N-dimethylaniline. Canonical SMILES: CC(C)(C)P(C1=CC=CC=C1C2=CC=CC=C2N(C)C)C(C)(C)C. Product ID: ACM224311493. Alfa Chemistry ISO 9001:2015 Certified. Categories: 2-di-tert-butylphosphino-2'-(N,N-dimethylamino)biphenyl. | |
| Tris(triphenylphosphine)rhodium(I) chloride | 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: Salt. Alternative Names: Chlorotris- (triphenylphosphino)-rhodium. CAS No. 14694-95-2. Product ID: rhodium; triphenylphosphane; chloride. Molecular formula: 925.21. Mole weight: C54H45ClP3Rh. 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=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. QBERHIJABFXGRZ-UHFFFAOYSA-M. 98%. | |
| Tyloxapol | Tyloxapol is a nonionic liquid polymer of the alkyl aryl polyether alcohol type, used as a surface active stabilizer. Tyloxapol is used to induce hyperlipidemia in animals [1] [2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 25301-02-4. Pack Sizes: 500 mg; 1 g. Product ID: HY-B1068. | |
| Tyloxapol | Tyloxapol. Uses: Tyloxapol, is a nonionic liquid polymer of the alkyl aryl polyether alcohol type. it is used as a surfactant to aid liquefaction and removal of mucopurulent (containing mucus and pus) bronchopulmonary secretions. tyloxapol also blocks plasma lipolytic activity. Group: Polymers. Alternative Names: Ethoxylated p-tert-octylphenol formaldehyde polymer. CAS No. 25301-02-4. Product ID: formaldehyde; oxirane; 4-(2,4,4-trimethylpentan-2-yl)phenol. Molecular formula: 137.18. Mole weight: C8H11NO. CC(C)(C)CC(C)(C)C1=CC=C(C=C1)O. C=O. C1CO1. InChI=1S/C14H22O.C2H4O.CH2O/c1-13(2, 3)10-14(4, 5)11-6-8-12(15)9-7-11; 1-2-3-1; 1-2/h6-9, 15H, 10H2, 1-5H3; 1-2H2; 1H2. MDYZKJNTKZIUSK-UHFFFAOYSA-N. 99%. | |
| Tyloxapol, USP | Tyloxapol is a nonionic liquid polymer of the alkyl aryl polyether alcohol type. It is used as a surfactant to aid liquefaction and removal of mucopurulent[citation needed] (containing mucus and pus) bronchopulmonary secretions,[1][2] administered by inhalation through a nebulizer[3] or with a stream of oxygen. With intraperitoneal injection, tyloxapol also blocks plasma lipolytic activity, and thus the breakdown of triglyceride-rich lipoproteins. This mechanism is used to induce experimental hyperlipidemia in animals.[4] Tyloxapol is the main active ingredient of the medical device Tacholiquin®. Tacholiquin® is an expectorant designated for inhalation and instillation reaching the upper and lower airways. Group: Biochemicals. Alternative Names: p- (1, 1, 3, 3-Tetramethylbutyl) Phenol Polymer with Ethylene Oxide and Formaldehyde; Ethylene Oxide Polymer with Formaldehyde and p- (1, 1, 3, 3-Tetramethylbutyl) phenol; Oxirane Polymer with Formaldehyde and 4- (1, 1, 3, 3-tetramethylbutyl) phenol; Ethylene oxide-formaldehyde-4- (1, 1, 3, 3-tetramethylbutyl) phenol copolymer; Ethylene oxide-formaldehyde-p-octylphenol Copolymer; NSC 90255; Superinone; Triton A 20; Triton WR 1339; Tyloxapol; p-Isooctyl polyoxyethyl ene phenol Formaldehyde Polymer. Grades: USP. CAS No. 25301-02-4. Pack Sizes: 1g, 5g, 25g. Molecular Formula: (C17H30O4)n, Molecular Weight: As reported. US Biological Life Sciences. | Worldwide |
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