Androst-5-en-17-one, 3,16-bis(acetyloxy)-, (3beta,16beta)-

Base Information

Chemical Name:Androst-5-en-17-one, 3,16-bis(acetyloxy)-, (3beta,16beta)-
CAS No.:16597-57-2
Molecular Formula:C₂₃H₃₂O₅
Molecular Weight:388.504
Hs Code.:
DSSTox Substance ID:DTXSID10563934
Nikkaji Number:J131.277D
Wikidata:Q82448465
Mol file:16597-57-2.mol

Synonyms:16597-57-2;Androst-5-en-17-one, 3,16-bis(acetyloxy)-, (3beta,16beta)-;[(3S,8R,9S,10R,13S,14S,16S)-16-acetyloxy-10,13-dimethyl-17-oxo-1,2,3,4,7,8,9,11,12,14,15,16-dodecahydrocyclopenta[a]phenanthren-3-yl] acetate;DTXSID10563934;RWUHRLQWZKUBTF-HVWUICSASA-N;Androst-5-en-17-one, 3,16-bis(acetyloxy)-, (3.beta.,16.beta.)-;16-(Acetyloxy)-17-oxoandrost-5-en-3-yl acetate #;(3beta,16beta)-17-Oxoandrost-5-ene-3,16-diyl diacetate;[(3S,8R,9S,10R,13S,14S,16S)-16-acetoxy-10,13-dimethyl-17-oxo-1,2,3,4,7,8,9,11,12,14,15,16-dodecahydrocyclopenta[a]phenanthren-3-yl] acetate

Suppliers and Price of Androst-5-en-17-one, 3,16-bis(acetyloxy)-, (3beta,16beta)-

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 2 raw suppliers

Chemical Property of Androst-5-en-17-one, 3,16-bis(acetyloxy)-, (3beta,16beta)-

Chemical Property:

PSA：69.67000
LogP:3.99160
XLogP3:3.8
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:4
Exact Mass:388.22497412
Heavy Atom Count:28
Complexity:739

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

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(=O)OC1CCC2(C3CCC4(C(C3CC=C2C1)CC(C4=O)OC(=O)C)C)C
Isomeric SMILES:CC(=O)O[C@H]1CC[C@@]2([C@H]3CC[C@]4([C@H]([C@@H]3CC=C2C1)C[C@@H](C4=O)OC(=O)C)C)C

Technology Process of Androst-5-en-17-one, 3,16-bis(acetyloxy)-, (3beta,16beta)-

There total 11 articles about Androst-5-en-17-one, 3,16-bis(acetyloxy)-, (3beta,16beta)- 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: 62.0%

: 25256-95-5
3β,17β-Diacetoxy-androsta-5,16-diene

: 108-24-7
acetic anhydride

: 10587-75-4,16597-57-2
3beta,16beta-Diacetoxyandrost-5-en-17-one

: 378223-43-9
3β-acetoxy-16β-(acetoxy)acetoxyandrost-5-en-17-one

Guidance literature:: With lead(IV) acetate; acetic acid; at 20 ℃;
DOI:10.1016/S0039-128X(01)00103-9

Reference yield:

: 96442-97-6
3β,16β-Diacetoxy-5α,6β-dichlor-androstan-17-on

: 10587-75-4,16597-57-2
3beta,16beta-Diacetoxyandrost-5-en-17-one

Guidance literature:: With acetic acid; zinc; In acetic acid;
DOI:10.1248/cpb.12.808

Reference yield:

: 17975-95-0
5α,6β-dichloroandrost-16-en-3β,17-diol diacetate

: 10587-75-4,16597-57-2
3beta,16beta-Diacetoxyandrost-5-en-17-one

Guidance literature:: Multi-step reaction with 2 steps

1: Pb(OAc)4 / acetic acid

2: Zn, AcOH / acetic acid

With lead(IV) acetate; acetic acid; zinc; In acetic acid;
DOI:10.1248/cpb.12.808