Cholestan-3-ol

Base Information

Chemical Name:Cholestan-3-ol
CAS No.:27409-41-2
Molecular Formula:C27H48 O
Molecular Weight:388.678
Hs Code.:
DSSTox Substance ID:DTXSID90859347
Nikkaji Number:J1.236.505E
ChEMBL ID:CHEMBL69164
Mol file:27409-41-2.mol

Synonyms:5 alpha Cholestan 3 alpha ol;5 alpha Cholestan 3 beta ol;5 alpha-Cholestan-3 alpha-ol;5 alpha-Cholestan-3 beta-ol;5 beta Cholestan 3 beta ol;5 beta-Cholestan-3 alpha-ol;5 beta-Cholestan-3 beta-ol;beta Cholestanol;beta-Cholestan-3 beta-ol, 5;beta-Cholestanol;beta-ol, 5 beta-Cholestan-3;Cholestan 3 ol;Cholestan-3-ol;Cholestanol;Cholestanol, (3alpha, 5beta)-Isomer;Coprostanol;Coprosterol;Dihydrocholesterol

Suppliers and Price of Cholestan-3-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
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price

Total 0 raw suppliers

Chemical Property of Cholestan-3-ol

Chemical Property:

Boiling Point:455.5°Cat760mmHg
Flash Point:190.7°C
PSA：20.23000
Density:0.956g/cm³
LogP:7.46860
XLogP3:9.4
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:5
Exact Mass:388.370516150
Heavy Atom Count:28
Complexity:540

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(C)CCCC(C)C1CCC2C1(CCC3C2CCC4C3(CCC(C4)O)C)C
Isomeric SMILES:C[C@H](CCCC(C)C)[C@H]1CC[C@@H]2[C@@]1(CC[C@H]3[C@H]2CCC4[C@@]3(CCC(C4)O)C)C

Technology Process of Cholestan-3-ol

There total 55 articles about Cholestan-3-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: 100.0%

: 111222-20-9
2-[(3S,5R,8R,9S,10S,13R,14S,17R)-17-((R)-1,5-Dimethyl-hexyl)-10,13-dimethyl-hexadecahydro-cyclopenta[a]phenanthren-3-yloxy]-tetrahydro-furan

: 80-97-7,360-68-9,516-92-7,516-95-0,566-84-7,14615-12-4,16720-60-8,17608-41-2,18769-46-5,27409-41-2,56193-35-2,57759-49-6,73465-18-6,103365-91-9,105119-51-5
Coprostanol

Guidance literature:: With toluene-4-sulfonic acid; In ethanol; for 1h; Ambient temperature;
DOI:10.1055/s-1987-27903

Reference yield: 97.0%

: 4-[(3S,5R,8R,9S,10S,13R,14S,17R)-17-((R)-1,5-Dimethyl-hexyl)-10,13-dimethyl-hexadecahydro-cyclopenta[a]phenanthren-3-yloxymethyl]-benzonitrile

: 80-97-7,360-68-9,516-92-7,516-95-0,566-84-7,14615-12-4,16720-60-8,17608-41-2,18769-46-5,27409-41-2,56193-35-2,57759-49-6,73465-18-6,103365-91-9,105119-51-5
Coprostanol

Guidance literature:: With Triethylgermyl-natrium; In 1,4-dioxane; N,N,N,N,N,N-hexamethylphosphoric triamide; at 50 ℃; for 15h;
DOI:10.1246/cl.2002.1032

Reference yield: 84.0%

: Trifluoro-methanesulfonic acid (3S,5R,8R,9S,10S,13R,14S,17R)-17-((R)-1,5-dimethyl-hexyl)-10,13-dimethyl-hexadecahydro-cyclopenta[a]phenanthren-3-yl ester

: 80-97-7,360-68-9,516-92-7,516-95-0,566-84-7,14615-12-4,16720-60-8,17608-41-2,18769-46-5,27409-41-2,56193-35-2,57759-49-6,73465-18-6,103365-91-9,105119-51-5
Coprostanol

Guidance literature:: With 18-crown-6 ether; cesium acetate; In benzene; for 24h; Product distribution; Heating;
DOI:10.1016/0040-4039(96)01333-0