Home > Compound List > Product Information
11α-Hydroxy Canrenone_Molecular_structure_CAS_192569-17-8)
Click picture or here to close

11α-Hydroxy Canrenone

Catalog No. H883500 Name Toronto Research Chemicals
CAS Number 192569-17-8 Website http://www.trc-canada.com
M. F. C22H28O4 Telephone +1 (416) 665-9696
M. W. 356.45532 Fax +1 (416) 665-4439
Purity Email info@trc-canada.com
Storage -20°C Freezer Chembase ID: 170318

SYNONYMS

IUPAC name
(2R,2'R,15'S,17'R)-17'-hydroxy-2',15'-dimethylspiro[oxolane-2,14'-tetracyclo[8.7.0.02,7.011,15]heptadecane]-6',8'-diene-5,5'-dione
IUPAC Traditional name
(2R,2'R,15'S,17'R)-17'-hydroxy-2',15'-dimethylspiro[oxolane-2,14'-tetracyclo[8.7.0.02,7.011,15]heptadecane]-6',8'-diene-5,5'-dione
Synonyms
(11α,17α)-11,17-Dihydroxy-3-oxopregna-4,6-diene-21-carboxylic Acid γ-Lactone

DATABASE IDS

CAS Number 192569-17-8

PROPERTIES

Certificate of Analysis Download
Apperance Yellow Solid
Melting Point 232-234°C
Solubility Acetone
Solubility Chloroform
Solubility Methanol
MSDS Link Download
Storage Condition -20°C Freezer

DETAILS

Description (English)
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.

REFERENCES

  • Luetscher, J., et al.: J. Clin. Invest., 29, 1576 (1950)
  • Gaunt, R., et al.: J. Clin. Endocrinol. Metab., 15, 621 (1950)
  • McMahon, E., et al.: Curr. Opin. Pharm., 1, 190 (1950)
  • McMahon, E., et al.: Curr. Pharm. Des., 9, 1065 (1950)