3β-(Acetyloxy)-5-hydroxy-5β-androstane-17β-carboxylic acid methyl ester

Base Information

Chemical Name:3β-(Acetyloxy)-5-hydroxy-5β-androstane-17β-carboxylic acid methyl ester
CAS No.:55956-03-1
Molecular Formula:
Molecular Weight:392.53
Hs Code.:
Mol file:55956-03-1.mol

Synonyms:3β-(Acetyloxy)-5-hydroxy-5β-androstane-17β-carboxylic acid methyl ester

Suppliers and Price of 3β-(Acetyloxy)-5-hydroxy-5β-androstane-17β-carboxylic acid methyl ester

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of 3β-(Acetyloxy)-5-hydroxy-5β-androstane-17β-carboxylic acid methyl ester

Chemical Property:

Purity/Quality:

Safty Information:

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MSDS Files:

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Technology Process of 3β-(Acetyloxy)-5-hydroxy-5β-androstane-17β-carboxylic acid methyl ester

There total 7 articles about 3β-(Acetyloxy)-5-hydroxy-5β-androstane-17β-carboxylic acid methyl ester which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

: 55956-03-1,96611-84-6
3β-Acetoxy-5β-hydroxy-aetiansaeure-methylester

Guidance literature:: With acetic acid; platinum; Hydrogenation;
DOI:10.1002/hlca.19490320423

Reference yield:

: 55956-03-1,96611-84-6
5-hydroxy-3β-acetoxy-21-nor-5α.14β.17βH-pregnanoic acid-(20)-methyl ester

Guidance literature:: With acetic acid; platinum; Hydrogenation;
DOI:10.1002/hlca.19490320423

Reference yield:

: 5.21-dihydroxy-3β-acetoxy-5β-pregnen-(14)-one-(20)

: 55956-03-1
5-hydroxy-3β-acetoxy-21-nor-5β-pregnanoic acid-(20)-methyl ester

Guidance literature:: With 1,4-dioxane; periodic acid; Behandlung des Reaktionsprodukts mit Diazomethan in Aether und Hydrierung des danach isolierten Esters an Platin in Essigsaeure;
DOI:10.1002/hlca.19490320519