Doristerol

Base Information

Chemical Name:Doristerol
CAS No.:566-99-4
Molecular Formula:C27H46O
Molecular Weight:386.662
Hs Code.:
UNII:TPL64BMT8B
DSSTox Substance ID:DTXSID901312065
Nikkaji Number:J144.723H
Wikidata:Q76294384
Metabolomics Workbench ID:34403
Mol file:566-99-4.mol

Synonyms:Doristerol;566-99-4;Cholest-8(14)-en-3beta-ol;(3S,5S,9R,10S,13R,17R)-10,13-dimethyl-17-[(2R)-6-methylheptan-2-yl]-2,3,4,5,6,7,9,11,12,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol;5alpha-Cholest-8(14)-en-3beta-ol;LMST01010097;SCHEMBL4303282;5a-cholest-8(14)-en-3b-ol;CHEBI:166793;DTXSID901312065

Suppliers and Price of Doristerol

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 4 raw suppliers

Chemical Property of Doristerol

Chemical Property:

Melting Point:114-116°C
PSA：20.23000
LogP:7.53280
Storage Temp.:Refrigerator, under inert atmosphere
Solubility.:Chloroform (Slightly), Methanol (Slightly, Heated)
XLogP3:8
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:5
Exact Mass:386.354866087
Heavy Atom Count:28
Complexity:603

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(C)CCCC(C)C1CCC2=C3CCC4CC(CCC4(C3CCC12C)C)O
Isomeric SMILES:C[C@H](CCCC(C)C)[C@H]1CCC2=C3CC[C@H]4C[C@H](CC[C@@]4([C@H]3CC[C@]12C)C)O
Uses Doristerol is a sterol lipid molecule. An unsaturated sterol intermediate.

Technology Process of Doristerol

There total 25 articles about Doristerol 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: 35.0%