12α-hydroxy-5β-cholan-24-oic acid

Base Information

Chemical Name:12α-hydroxy-5β-cholan-24-oic acid
CAS No.:15173-22-5
Molecular Formula:C₂₄H₄₀O₃
Molecular Weight:376.58
Hs Code.:

Synonyms:

Suppliers and Price of 12α-hydroxy-5β-cholan-24-oic acid

Supply Marketing:

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

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 2 raw suppliers

Chemical Property of 12α-hydroxy-5β-cholan-24-oic acid

Chemical Property:

Purity/Quality:: 95%+ or 98%+ ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Uses 12α-Hydroxycholanoic Acid can be used to analyze the degradation of?desoxycholic acid side chain. It can also be utilized as a substrate to study the stereospecificity of 3α-hydroxysteroid dehydrogenase.

Technology Process of 12α-hydroxy-5β-cholan-24-oic acid

There total 2 articles about 12α-hydroxy-5β-cholan-24-oic acid 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:

: 15152-40-6,15173-22-5,15173-23-6,30627-80-6,77059-18-8,106862-78-6
12α-Hydroxy-cholansaeure

Guidance literature:: 12-Oxo-cholansaeure, Li in fl.NH3+Propanol od. Na in Propanol;

Reference yield:

: 15152-40-6,15173-22-5,15173-23-6,30627-80-6,77059-18-8,106862-78-6
12α-Hydroxycholansaeure

Guidance literature:: 3-Keto-12α-hydroxycholansaeure -> solvatierte Verb.;
DOI:10.1021/bi00829a056

Reference yield:

: 15173-22-5
12α-hydroxy-5β-cholan-24-oic acid

: 1173-30-4
12-keto-5β-cholan-24-oic acid methyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: Jones' reagent / acetone / 0.08 h

With jones' reagent; In acetone;
DOI:10.1021/jo020146b