CAS 24637-46-5
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8 produtos.
(R)-4-((3R,5R,8S,10S,12S,13R,14S,17R)-3,12-Dihydroxy-10,13-dimethyl-2,3,4,5,6,7,8,10,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl)pentanoic acid
CAS:Fórmula:C24H38O4Pureza:98%Cor e Forma:SolidPeso molecular:390.5561(R)-4-((3R,5R,8S,10S,12S,13R,14S,17R)-3,12-Dihydroxy-10,13-dimethyl-2,3,4,5,6,7,8,10,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl)pentanoic acid
CAS:(R)-4-((3R,5R,8S,10S,12S,13R,14S,17R)-3,12-Dihydroxy-10,13-dimethyl-2,3,4,5,6,7,8,10,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl)pentanoic acidPureza:95%Peso molecular:390.56g/mol3Alpha,12Alpha-Dihydroxy-5Beta-chol-9(11)-enic Acid
CAS:Applications 3α,12α-Dihydroxy-5β-chol-9(11)-enic Acid is used in the analysis and in the structure determination of unsaturated 5β-cholanoic acids.
References Kuksis, A., et al.: Lipids, 15, 770 (1980)Fórmula:C24H38O4Cor e Forma:White To Off-WhitePeso molecular:390.56(3alpha,5beta,7alpha,24E)-3,7-Dihydroxy-cholest-24-en-26-oic Acid
CAS:Produto ControladoApplications (3α,5β,7α,24E)-3,7-Dihydroxy-cholest-24-en-26-oic acid is used in the preparation of a nonstereospecific 3α,7α,24-trihydroxy-5β-cholestan-26-oic acid during chenodeoxycholic acid biosynthesis, which has been identified as a key intermediate in chenodeoxycholic acid biosynthesis.
References Kobayashi, N.; et al.: Chem. Pharm. Bull, 42, 1536 (1994)Fórmula:C24H38O4Cor e Forma:NeatPeso molecular:390.563α,12α-Dihydroxy-5β-chol-9(11)-enic acid
CAS:Produto ControladoPlease enquire for more information about 3α,12α-Dihydroxy-5β-chol-9(11)-enic acid including the price, delivery time and more detailed product information at the technical inquiry form on this pageFórmula:C24H38O4Pureza:Min. 95%Cor e Forma:PowderPeso molecular:390.6 g/molRef: 3D-ZAA63746
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