testosterone (E)-3-(O-carboxymethyl)oxime

Base Information

Chemical Name:testosterone (E)-3-(O-carboxymethyl)oxime
CAS No.:58116-37-3
Molecular Formula:C₂₁H₃₁NO₄
Molecular Weight:361.481
Hs Code.:
European Community (EC) Number:634-429-5
UNII:0D98SO4W7H
Metabolomics Workbench ID:61045,61046
Nikkaji Number:J1.126.955I,J355.535F
Wikidata:Q27127171

Synonyms:testosterone (E)-3-(O-carboxymethyl)oxime;syn-testosterone-3-CMO;(Z)-testosterone-3-CMO;0D98SO4W7H;testosterone (Z)-3-(O-carboxymethyl)oxime;Testosterone 3-(O-(carboxymethyl)oxime), (Z)-;2-[(Z)-[(8R,9S,10R,13S,14S,17S)-17-hydroxy-10,13-dimethyl-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-ylidene]amino]oxyacetic acid;58116-37-3;({[(3Z)-17beta-hydroxyandrost-4-en-3-ylidene]amino}oxy)acetic acid;10190-93-9;CHEBI:60293;CHEBI:60294;Epitope ID:136784;17Beta-hydroxy-4-androsten-3-one 3-[o-carboxymethyl]oxime;UNII-0D98SO4W7H;2-({[(1S,3aS,3bR,9aR,9bS,11aS)-1-hydroxy-9a,11a-dimethyl-1H,2H,3H,3aH,3bH,4H,5H,7H,8H,9H,9aH,9bH,10H,11H,11aH-cyclopenta[a]phenanthren-7-ylidene]amino}oxy)acetic acid;Q27127171;Acetic acid, ((((3Z,17beta)-17-hydroxyandrost-4-en-3-ylidene)amino)oxy)-;ACETIC ACID, ((((3Z,17.BETA.)-17-HYDROXYANDROST-4-EN-3-YLIDENE)AMINO)OXY)-

Suppliers and Price of testosterone (E)-3-(O-carboxymethyl)oxime

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of testosterone (E)-3-(O-carboxymethyl)oxime

Chemical Property:

XLogP3:3.5
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:3
Exact Mass:361.22530847
Heavy Atom Count:26
Complexity:656

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MSDS Files:

Useful:

Canonical SMILES:CC12CCC3C(C1CCC2O)CCC4=CC(=NOCC(=O)O)CCC34C
Isomeric SMILES:C[C@]12CC[C@H]3[C@H]([C@@H]1CC[C@@H]2O)CCC4=C/C(=N\OCC(=O)O)/CC[C@]34C

Technology Process of testosterone (E)-3-(O-carboxymethyl)oxime

There total 2 articles about testosterone (E)-3-(O-carboxymethyl)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:

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