3beta-Hydroxy-5-androsten-17-one oxime

Base Information

Chemical Name:3beta-Hydroxy-5-androsten-17-one oxime
CAS No.:2830-48-0
Molecular Formula:C₁₉H₂₉NO₂
Molecular Weight:303.445
Hs Code.:
DSSTox Substance ID:DTXSID40418887
ChEMBL ID:CHEMBL2262587
Mol file:2830-48-0.mol

Synonyms:CHEMBL2262587;DTXSID40418887;WNJVMVZIGIACNN-KFAXOAFNSA-N;3.beta.-Hydroxy-5-androsten-17-one oxime;(3S,8R,9S,10R,13S,14S,17Z)-17-hydroxyimino-10,13-dimethyl-1,2,3,4,7,8,9,11,12,14,15,16-dodecahydrocyclopenta[a]phenanthren-3-ol

Suppliers and Price of 3beta-Hydroxy-5-androsten-17-one oxime

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 9 raw suppliers

Chemical Property of 3beta-Hydroxy-5-androsten-17-one oxime

Chemical Property:

Vapor Pressure:0mmHg at 25°C
Boiling Point:462.2°Cat760mmHg
Flash Point:304.4°C
Density:1.3g/cm³
XLogP3:3.5
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:0
Exact Mass:303.219829168
Heavy Atom Count:22
Complexity:540

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC12CCC3C(C1CCC2=NO)CC=C4C3(CCC(C4)O)C
Isomeric SMILES:C[C@]1\2CC[C@H]3[C@H]([C@@H]1CC/C2=N\O)CC=C4[C@@]3(CC[C@@H](C4)O)C

Technology Process of 3beta-Hydroxy-5-androsten-17-one oxime

There total 7 articles about 3beta-Hydroxy-5-androsten-17-one oxime 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: 97.22%

: 53-43-0
dehydroepiandrosterone

: 1232-19-5,13996-45-7,2830-48-0
17-hydroxyiminoandrost-5-en-3β-ol

Guidance literature:: With sulfuric acid; hydrazine hydrate; In ethanol; at 20 ℃; for 35h;

Reference yield:

: 84368-89-8,106294-20-6,119907-02-7,21063-30-9
3β-acetoxy-androst-5-en-17-one oxime

: 1232-19-5,13996-45-7,2830-48-0
17-hydroxyiminoandrost-5-en-3β-ol

Guidance literature:: With methanol; potassium hydroxide;

Reference yield:

: 853-23-6
prasterone acetate

: 1232-19-5,13996-45-7,2830-48-0
17-hydroxyiminoandrost-5-en-3β-ol

Guidance literature:: Multi-step reaction with 2 steps

1: hydroxylamine hydrochloride

2: methanol; potassium hydroxide

With methanol; hydroxylamine hydrochloride; potassium hydroxide;
DOI:10.1007/s00044-010-9393-3