Campesteryl acetate

Base Information

Chemical Name:Campesteryl acetate
CAS No.:1900-53-4
Molecular Formula:C30H50 O2
Molecular Weight:442.726
Hs Code.:
UNII:7PG68X5ECI
Nikkaji Number:J2.124.607G
Wikidata:Q27268679
Mol file:1900-53-4.mol

Synonyms:Campesteryl acetate;Campesterol acetate;Campesterol, acetate;1900-53-4;UNII-7PG68X5ECI;7PG68X5ECI;Ergost-5-en-3-ol, acetate, (3beta,24R)-;Ergost-5-en-3-ol, 3-acetate, (3beta,24R)-;Ergost-5-en-3-ol, acetate, (3.beta.,24R)-;[(3S,8S,9S,10R,13R,14S,17R)-17-[(2R,5R)-5,6-dimethylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl] acetate;Ergost-5-en-3-yl acetate #;SCHEMBL4735279;Q27268679;ERGOST-5-EN-3-OL, 3-ACETATE, (3.BETA.,24R)-

Suppliers and Price of Campesteryl acetate

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 7 raw suppliers

Chemical Property of Campesteryl acetate

Chemical Property:

PSA：26.30000
LogP:8.20550
XLogP3:9.4
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:7
Exact Mass:442.381080833
Heavy Atom Count:32
Complexity:722

Purity/Quality:: 98%,99%, ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC(=O)C)C)C
Isomeric SMILES:C[C@H](CC[C@@H](C)C(C)C)[C@H]1CC[C@@H]2[C@@]1(CC[C@H]3[C@H]2CC=C4[C@@]3(CC[C@@H](C4)OC(=O)C)C)C

Technology Process of Campesteryl acetate

There total 43 articles about Campesteryl acetate 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: 91.0%

: 1251919-63-7
C₃₀H₅₀O₃

: 1900-53-4
campesteryl acetate

Guidance literature:: With aluminium(III) iodide; In dichloromethane; acetonitrile; at 20 ℃; for 0.666667h;
DOI:10.1016/j.steroids.2010.05.016