5β-Cholan-3α-ol

Base Information

Chemical Name:5β-Cholan-3α-ol
CAS No.:5352-77-2
Molecular Formula:C24H42O
Molecular Weight:346.59
Hs Code.:
Mol file:5352-77-2.mol

Synonyms:5β-Cholan-3α-ol;(3R,5R,8R,9S,10S,13R,14S,17R)-10,13-Dimethyl-17-((R)-1-methyl-butyl)-hexadecahydro-cyclopenta[a]phenanthren-3-ol;

Suppliers and Price of 5β-Cholan-3α-ol

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 3 raw suppliers

Chemical Property of 5β-Cholan-3α-ol

Chemical Property:

Melting Point:143 - 144 °C (H2O)
Boiling Point:428.4±13.0 °C(Predicted)
PKA:15.14±0.70(Predicted)
PSA：20.23000
Density:0.972±0.06 g/cm3(Predicted)
LogP:6.44240

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 5β-Cholan-3α-ol

There total 9 articles about 5β-Cholan-3α-ol 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: 65.0%

: 113466-05-0
Methanesulfonic acid (R)-4-((3R,5R,8R,9S,10S,13R,14S,17R)-3-hydroxy-10,13-dimethyl-hexadecahydro-cyclopenta[a]phenanthren-17-yl)-pentyl ester

: 5352-77-2
(3α,5β)-cholan-3-ol

: 20414-15-7,101046-88-2,20414-16-8
5β-cholane-3α,24-diol

Guidance literature:: With potassium Sodium; tert-butyl alcohol; Tris(3,6-dioxaheptyl)amine; In tetrahydrofuran; Ambient temperature; var. cat.: 18-crown-6;
DOI:10.1016/S0040-4039(00)95452-2

Reference yield:

: 20414-15-7,101046-88-2,20414-16-8
5β-cholane-3α,24-diol

: 5352-77-2
(3α,5β)-cholan-3-ol

Guidance literature:: Multi-step reaction with 2 steps

2: LiAlH₄; diethyl ether

With lithium aluminium tetrahydride; diethyl ether;
DOI:10.1079/AHRR200236