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ChemicalBook--->CAS DataBase List--->192704-56-6

192704-56-6

192704-56-6 Structure

192704-56-6 Structure
IdentificationBack Directory
[Name]

11-a-Hydroxy canrenone methyl ester
[CAS]

192704-56-6
[Synonyms]

11α-HydroxyMexrenone
11α-Hydroxy Mexrenone
11a-Hydroxy Mexrenone
11alpha-Hydroxymexrenone
11α-Hydroxymexrenone(A2)
Eplerenone intermediate A2
11α-HydroxEplerenone Impurity
Eplerenone 11α-Hydroxy Analog
Eplerenone 11α-Hydroxy Analog
11α-Hydroxy canrenone methyl ester
Eplerenone 11-alpha-Hydroxy Analog
11-a-Hydroxy canrenone methyl ester
11-Alpha-Hydroxy canrenone methyl ester
TIANFU-CHEM 11-a-Hydroxy canrenone methyl ester
11α,17β-Dihydroxypregn-4-en-3-one 7α,21-dicarboxylic Acid γ-Lactone Methyl Ester
11-ALPHA-HYDROXY-7-ALPHA-(METHOXYCARBONYL)-3-OXOPREGN-4-ENE-21,17-ALPHA-CARBOLACTONE
(7α,11α,17α)-11,17-Dihydroxy-3-oxopregn-4-ene-7,21-dicarboxylic Acid γ-Lactone Methyl Ester
Pregn-4-ene-7,21-dicarboxylicacid, 11,17-dihydroxy-3-oxo-, g-lactone, methyl ester, (7a,11a,17a)-
Pregn-4-ene-7,21-dicarboxylic acid, 11,17-dihydroxy-3-oxo-, γ-lactone, methyl ester, (7α,11α,17α)-
methyl (7R,8S,9S,10R,11R,13S,14S,17R)-11-hydroxy-10,13-dimethyl-3,5'-dioxospiro[2,6,7,8,9,11,12,14,15,16-decahydro-1H-cyclopenta[a]phenanthrene-17,2'-oxolane]-7-carboxylate
[EINECS(EC#)]

206-141-6
[Molecular Formula]

C24H32O6
[MDL Number]

MFCD18252911
[MOL File]

192704-56-6.mol
[Molecular Weight]

416.507
Chemical PropertiesBack Directory
[Boiling point ]

604.5±55.0 °C(Predicted)
[density ]

1.27±0.1 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,Room Temperature
[solubility ]

Chloroform (Slightly), DMSO (Slightly), Methanol (Slightly)
[form ]

Solid
[pka]

14.40±0.70(Predicted)
[color ]

White to Off-White
[Stability:]

Hygroscopic
[InChIKey]

ZYDNRZOTRVTMRC-ROUXWHDHNA-N
[SMILES]

C1[C@]2(C)[C@@]3([H])[C@H](O)C[C@]4(C)[C@]5(CCC(=O)O5)CC[C@@]4([H])[C@]3([H])[C@H](C(OC)=O)CC2=CC(=O)C1 |&1:1,3,5,8,10,18,20,22,r|
[CAS DataBase Reference]

192704-56-6
Hazard InformationBack Directory
[Uses]

11a-Hydroxy Mexrenone is an intermediate used in the chemobiological synthesis of Eplerenone (E588775), a cardiovascular drug.
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