Epoxideoxycorticosterone acetate

Base Information

Chemical Name:Epoxideoxycorticosterone acetate
CAS No.:21853-83-8
Molecular Formula:C23H30 O5
Molecular Weight:386.488
Hs Code.:
European Community (EC) Number:244-620-1
NSC Number:18316
UNII:ZM67E95910
DSSTox Substance ID:DTXSID901188674
Nikkaji Number:J225.462J
Wikidata:Q27115867
Mol file:21853-83-8.mol

Synonyms:Epoxideoxycorticosterone acetate;21853-83-8;NSC-18316;ZM67E95910;[2-[(1R,2S,4R,6S,7S,10S,11R)-7,11-dimethyl-14-oxo-5-oxapentacyclo[8.8.0.02,7.04,6.011,16]octadec-15-en-6-yl]-2-oxoethyl] acetate;16alpha,17alpha-Epoxy-3,20-dioxopregn-4-en-21-yl acetate;16-alpha,17-alpha-Epoxy-3,20-dioxopregn-4-en-21-yl acetate;16,17-Epoxydeoxycorticosterone acetate;16,20-dione-21-acetate;UNII-ZM67E95910;CHEBI:34170;DTXSID901188674;NSC18316;SKF-3138;EINECS 244-620-1;NSC 18316;AKOS015955644;2-((6aR,6bS,8aS,8bS,9aR,10aS,10bR)-6a,8a-dimethyl-4-oxo-2,4,5,6,6a,6b,7,8,8a,8b,9a,10,10a,10b-tetradecahydro-1H-naphtho[2',1':4,5]indeno[1,2-b]oxiren-8b-yl)-2-oxoethyl acetate;16,17-EPOXYDEOXYCORTICOSTERONEACETATE;21-Acetoxy-16alpha,17-epoxypregn-4-ene-3,20-dione;Q27115867;CORTICOSTERONE, 11-DEOXY-16.ALPHA.,17-EPOXY-, ACETATE;Pregn-4-ene-3, 21-(acetyloxy)-16,17-epoxy-, (16.alpha.)-;PREGN-4-ENE-3,20-DIONE, 16.ALPHA.,17-EPOXY-21-HYDROXY-, ACETATE;Pregn-4-ene-3,20-dione, 21-(acetyloxy)-16,17-epoxy-, (16.alpha.)-;Pregn-4-ene-3,20-dione, 21-(acetyloxy)-16,17-epoxy-, (16alpha)-;2-[(4aR,4bS,6aS,6bS,7aR,8aS,8bR)-4a,6a-dimethyl-2-oxo-2,3,4,4a,4b,5,6,6a,7a,8,8a,8b,9,10-tetradecahydro-6bH-naphtho[2',1':4,5]indeno[1,2-b]oxiren-6b-yl]-2-oxoethyl acetate

Suppliers and Price of Epoxideoxycorticosterone 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 Epoxideoxycorticosterone acetate

Chemical Property:

Boiling Point:523°Cat760mmHg
Flash Point:227.1°C
PSA：72.97000
Density:1.23g/cm³
LogP:3.39800
XLogP3:2.8
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:4
Exact Mass:386.20932405
Heavy Atom Count:28
Complexity:799

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

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(=O)OCC(=O)C12C(O1)CC3C2(CCC4C3CCC5=CC(=O)CCC45C)C
Isomeric SMILES:CC(=O)OCC(=O)[C@]12[C@H](O1)C[C@@H]3[C@@]2(CC[C@H]4[C@H]3CCC5=CC(=O)CC[C@]45C)C

Technology Process of Epoxideoxycorticosterone acetate

There total 6 articles about Epoxideoxycorticosterone 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: 67.0%