Identification | Back Directory | [Name]
Ethyl 3-Oxo-4-aza-5α-androst-1-ene-17β-carboxylate | [CAS]
157307-36-3 | [Synonyms]
Dutasteride EP Imp C Dutasteride Ethyl Ester Dutasteride EP Impurity C AHSRUURQZYMTKR-FKLRSJPUSA-N Dutasteride Impurity 6(Dutasteride EP Impurity C) Ethyl 3-Oxo-4-aza-5α-androst-1-ene-17β-carboxylate Ethyl 3-oxo-4-aza-5a-androst-1-ene-17b-carboxylate Ethyl 3-Oxo-4-aza-5α-androst-1-ene-17β-carboxylate Dutasteride EP Impurity C (Dutasteride Ethyl Ester) Ethyl 3-Oxo-4-aza-5a-androst-1-ene-17-Beta-carboxylate (4aR,4bS,6aS,7R,9aS,9bS,11aR)-ethyl 4a,6a-dimethyl-2-oxo-2,4a,4b,5,6,6a,7,8,9,9a,9b,10,11,11a-tetradecahydro-1H-indeno[5,4-f]quinoline-7-carboxylate (4aR,4bS,6aS,7S,9aS,9bS,11aR)-ethyl 4a,6a-dimethyl-2-oxo-2,4a,4b,5,6,6a,7,8,9,9a,9b,10,11,11a-tetradecahydro-1H-indeno[5,4-f]quinoline-7-carboxylate 1H-Indeno[5,4-f]quinoline-7-carboxylic acid, 2,4a,4b,5,6,6a,7,8,9,9a,9b,10,11,11a-tetradecahydro-4a,6a-dimethyl-2-oxo-, ethyl ester, (4aR,4bS,6aS,7S,9aS,9bS,11aR)- | [Molecular Formula]
C21H31NO3 | [MDL Number]
MFCD31562972 | [MOL File]
157307-36-3.mol | [Molecular Weight]
345.48 |
Chemical Properties | Back Directory | [Melting point ]
237 - 238°C | [Boiling point ]
489.9±45.0 °C(Predicted) | [density ]
1.099±0.06 g/cm3(Predicted) | [storage temp. ]
-20°C Freezer, Under inert atmosphere | [solubility ]
Chloroform (Slightly), DMSO (Slightly, Heated), Methanol (Slightly, Sonicated) | [form ]
Solid | [pka]
14.16±0.70(Predicted) | [color ]
White to Off-White |
Hazard Information | Back Directory | [Uses]
Ethyl 3-Oxo-4-aza-5α-androst-1-ene-17β-carboxylate (Dutateride EP Impurity C) is a compound synthesized in the production of azasteroids. Used in the inhibition of 5α-reductase and of androgen receptor binding, both major effecters in the male hormonal system. | [Uses]
Ethyl 3-Oxo-4-aza-5α-androst-1-ene-17β-carboxylate is a compound synthesized in the production of azasteroids. Used in the inhibition of 5α-reductase and of androgen receptor binding, both major effecters in the male hormonal system. |
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BOC Sciences
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16314854226 |
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www.bocsci.com |
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