11-alpha-Hydroxycarvenone Chemical Properties

Melting point:

232-234°C

Boiling point:

584.7±50.0 °C(Predicted)

Density 

1.25

storage temp. 

-20°C Freezer

solubility 

Chloroform (Slightly), Methanol (Slightly)

pka

14.55±0.60(Predicted)

form 

Solid

color 

Pale Yellow to Brown

InChI

InChI=1/C22H28O4/c1-20-8-5-14(23)11-13(20)3-4-15-16-6-9-22(10-7-18(25)26-22)21(16,2)12-17(24)19(15)20/h3-4,11,15-17,19,24H,5-10,12H2,1-2H3/t15-,16-,17+,19+,20-,21-,22+/s3

InChIKey

RJTDWMKVQUPGSY-IPRJTMRINA-N

SMILES

C[C@]12C[C@@H](O)[C@]3([H])[C@]4(CCC(=O)C=C4C=C[C@@]3([H])[C@]1([H])CC[C@]12CCC(=O)O1)C |&1:1,3,5,7,16,18,22,r|

CAS DataBase Reference

192569-17-8(CAS DataBase Reference)

11-alpha-Hydroxycarvenone Usage And Synthesis

Chemical Properties

Yellow Crystalline Solid

Uses

11α-Hydroxy Canrenone is the key intermediate in the synthesis of Eplerenone, a cardiovascular drug. Canrenone was biotransformed into 11α-Hydroxycanrenone by Aspergillus ochraceus SIT34205.

11-alpha-Hydroxycarvenone(192569-17-8)Related Product Information

• Hydroxy silicone oil
• Methylparaben
• 4-Hydroxybenzoic acid
• 4'-Hydroxyacetophenone
• Glycolic acid
• Hydroxyapatite
• Canrenone
• 4-Hydroxybenzaldehyde
• Ethyl 2-(Chlorosulfonyl)acetate
• 10-Hydroxycamptothecin
• Citric acid
• Folic acid
• Diethylstilbestrol
• 2'-Hydroxyacetophenone
• Ascoric Acid
• 11-a-Hydroxy canrenone methyl ester
• Delta 9,11-canrenone
• (7a,17a)-17-Hydroxy-3-oxo-pregna-4,9(11)-diene-7,21-dicarboxylicacid g-lactone methyl ester