Oxabolone

Base Information

• Chemical Name: Oxabolone
• CAS No.: 4721-69-1
• Molecular Formula: C18H26O3
• Molecular Weight: 290.403
• European Community (EC) Number: 225-212-2
• UNII: 51RPF719WE
• DSSTox Substance ID: DTXSID50878357
• Metabolomics Workbench ID: 146154
• Nikkaji Number: J11.017E
• Wikidata: Q7115044
• Wikipedia: Oxabolone
• Mol file: 4721-69-1.mol

Synonyms:Oxabolone;4-Hydroxy Nandrolone;4721-69-1;4-Hydroxy-19-nortestosterone;51RPF719WE;4-Hydroxynandrolone;(8R,9S,10R,13S,14S,17S)-4,17-dihydroxy-13-methyl-2,6,7,8,9,10,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-one;4-Hydroxy Nandrolone (1.0mg/ml in Acetonitrile);4,17beta-Dihydroxyestr-4-en-3-one;UNII-51RPF719WE;EINECS 225-212-2;OXABOLONE [MI];SCHEMBL151284;Estr-4-en-3-one, 4,17-dihydroxy-, (17.beta.)-;DTXSID50878357;CHEBI:135210;GXHBCWCMYVTJOW-YGRHGMIBSA-N;DB01500;Estr-4-en-3-one, 4,17beta-dihydroxy-;NS00044274;Estr-4-en-3-one, 4,17-dihydroxy-, (17beta)-;Q7115044

Chemical Property of Oxabolone

Chemical Property:

• Vapor Pressure: 3.02E-11mmHg at 25°C
• Melting Point: 188-190°
• Boiling Point: 480.4°Cat760mmHg
• Flash Point: 258.4°C
• PSA: 57.53000
• Density: 1.21g/cm³
• LogP: 3.37480
• XLogP3: 2.5
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 0
• Exact Mass: 290.18819469
• Heavy Atom Count: 21
• Complexity: 509

Purity/Quality:

99% ^*data from raw suppliers

4-HYDROXY-19-NORTESTOSTERONE 95.00% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC12CCC3C(C1CCC2O)CCC4=C(C(=O)CCC34)O
• Isomeric SMILES: C[C@]12CC[C@H]3[C@H]([C@@H]1CC[C@@H]2O)CCC4=C(C(=O)CC[C@H]34)O
• Uses: 4-Hydroxy Nandrolone is a metabolite of Nandrolone (N315000).

Technology Process of Oxabolone

There total 4 articles about Oxabolone 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:

norclostebol (13583-21-6) → 4-Hydroxy-19-nortestosterone (4721-69-1)

Guidance literature:

With potassium tert-butylate; In tert-butyl alcohol;

Reference yield:

→ 4-Hydroxy-19-nortestosterone (4721-69-1)

Guidance literature:

17β-Hydroxy-4ξ,5-epoxy-19-nor-5ξ-androstan-3-on, BF3-Etherat, Bzl.;

Reference yield:

→ 19-Nor-4-hydroxy-testosteron (4721-69-1)

Guidance literature:

19-Nor-4,5-Epoxy-androstan-17-ol-3-on, AcOH, TsOH/MeOH;

upstream raw materials:

norclostebol