Home > Name List By other > (7R,8R,9S,10R,13S,14S,17S)-17-hydroxy-7,13,17-trimethyl-1,2,6,7,8,9,10, 11,12,14,15,16-dodecahydrocyclopenta[a]phenanthren-3-...

CAS No 3704-09-4 , (7R,8R,9S,10R,13S,14S,17S)-17-hydroxy-7,13,17-trimethyl-1,2,6,7,8,9,10,
11,12,14,15,16-dodecahydrocyclopenta[a]phenanthren-3-one

  • Name: (7R,8R,9S,10R,13S,14S,17S)-17-hydroxy-7,13,17-trimethyl-1,2,6,7,8,9,10,
    11,12,14,15,16-dodecahydrocyclopenta[a]phenanthren-3-one
  • Synonyms: CDB 904; U-10,997; U 10997; 3704-09-4; Miboleronum;(7R,8R,9S,10R,13S,14S,17S)-17-hydroxy-7,13,17-trimethyl-1,2,6,7,8,9,10,
    11,12,14,15,16-dodecahydrocyclopenta[a]phenanthren-3-one; Miboleron; Cheque; CHEBI:34849;Mibolerona;
  • CAS Registry Number:
  • Flash Point: 187.8°C
  • Boiling Point: 440.5°Cat760mmHg
  • Density: 1.1g/cm3
  • Refractive index: 1.553
  • Safety Statements: Experimental teratogenic and reproductive effects. Questionable carcinogen with experimental neoplastigenic data. When heated to decomposition it emits acrid smoke and irritating fumes.
  • Flash Point: 187.8°C
  • EINECS: 223-046-5
  • Molecular Weight: 302.451
  • InchiKey: PTQMMNYJKCSPET-OMHQDGTGSA-N
  • InChI: InChI=1S/C20H30O2/c1-12-10-13-11-14(21)4-5-15(13)16-6-8-19(2)17(18(12)
    16)7-9-20(19,3)22/h11-12,15-18,22H,4-10H2,1-3H3/t12-,15+,16-,17+,18-,
    19+,20+/m1/s1
  • Molecular Formula: C20H30O2
  • Molecular Structure:CAS No:3704-09-4 (7R,8R,9S,10R,13S,14S,17S)-17-hydroxy-7,13,17-trimethyl-1,2,6,7,8,9,10,<br />11,12,14,15,16-dodecahydrocyclopenta[a]phenanthren-3-one

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    References of (7R,8R,9S,10R,13S,14S,17S)-17-hydroxy-7,13,17-trimethyl-1,2,6,7,8,9,10,
    11,12,14,15,16-dodecahydrocyclopenta[a]phenanthren-3-one
    Title: Mibolerone
    CAS Registry Number: 3704-09-4
    CAS Name: (7a,17b)-17-Hydroxy-7,17-dimethylestr-4-en-3-one
    Synonyms: 7a,17a-dimethyl-19-nortestosterone
    Manufacturers' Codes: U-10997
    Trademarks: Cheque
    Molecular Formula: C20H30O2
    Molecular Weight: 302.45
    Percent Composition: C 79.42%, H 10.00%, O 10.58%
    Literature References: Synthetic anabolic steroid related to testosterone, q.v. Prepn: BE 610385; J. C. Babcock, J. A. Campbell, US 3341557 (1962, 1967 both to Upjohn). Biological properties: J. A. Campbell et al., Steroids 1, 317 (1963). Dissolution and solubility rates: W. E. Hamlin et al., J. Pharm. Sci. 54, 1651 (1965). Pharmacodynamics: J. H. Sokolowski, C. W. Kasson, Am. J. Vet. Res. 39, 837 (1978). Efficacy evaluation in dogs: J. H. Sokolowski, J. Am. Vet. Med. Assoc. 173, 983 (1978).
    Properties: Cryst solid. Soly in deionized water: 0.0454 mg/ml at 37°.
    NOTE: This is a controlled substance (anabolic steroid): 21 CFR, 1308.13, as defined in 1300.01.
    Therap-Cat-Vet: Antigonadotropic used to suppress estrus.