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CAS No 53-39-4 , (1S,3aS,3bR,5aS,9aS,9bS,11aS)-1-hydroxy-1,9a,11a-trimethyl-2,3,3a,3b,4,
5,5a,6,9,9b,10,11-dodecahydroindeno[4,5-h]isochromen-7-one

  • Name: (1S,3aS,3bR,5aS,9aS,9bS,11aS)-1-hydroxy-1,9a,11a-trimethyl-2,3,3a,3b,4,
    5,5a,6,9,9b,10,11-dodecahydroindeno[4,5-h]isochromen-7-one
  • Synonyms: Oxandrolonum; Oxandrolona; Lonavar; Provitar; Ossandrolone [DCIT];(1S,3aS,3bR,5aS,9aS,9bS,11aS)-1-hydroxy-1,9a,11a-trimethyl-2,3,3a,3b,4,
    5,5a,6,9,9b,10,11-dodecahydroindeno[4,5-h]isochromen-7-one; Anavar;Oxandrin; Vasorome; Protivar;
  • CAS Registry Number:
  • Melting Point: 235-238 ºC
  • Flash Point: 179.1°C
  • Boiling Point: 444.4°Cat760mmHg
  • Density: 1.105g/cm3
  • Refractive index: 1.526
  • Water Solubility: very slightly soluble in water
  • Safety Statements: Moderately toxic by ingestion and intraperitoneal routes. Experimental reproductive effects. When heated to decomposition it emits acrid smoke and fumes.
  • Flash Point: 179.1°C
  • EINECS: 200-172-9
  • Molecular Weight: 306.4397
  • InchiKey: QSLJIVKCVHQPLV-PEMPUTJUSA-N
  • InChI: InChI=1S/C19H30O3/c1-17-11-22-16(20)10-12(17)4-5-13-14(17)6-8-18(2)15
    (13)7-9-19(18,3)21/h12-15,21H,4-11H2,1-3H3/t12-,13+,14-,15-,17-,18-,
    19-/m0/s1
  • Molecular Formula: C19H30O3
  • Molecular Structure:CAS No:53-39-4 (1S,3aS,3bR,5aS,9aS,9bS,11aS)-1-hydroxy-1,9a,11a-trimethyl-2,3,3a,3b,4,<br />5,5a,6,9,9b,10,11-dodecahydroindeno[4,5-h]isochromen-7-one

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References of (1S,3aS,3bR,5aS,9aS,9bS,11aS)-1-hydroxy-1,9a,11a-trimethyl-2,3,3a,3b,4,
5,5a,6,9,9b,10,11-dodecahydroindeno[4,5-h]isochromen-7-one
Title: Oxandrolone
CAS Registry Number: 53-39-4
CAS Name: (4aS,4bS,6aS,7S,9aS,9bR,11aS)-Tetradecahydro-7-hydroxy-4a,6a,7-trimethylcyclopenta[5,6]naphtho[1,2-c]pyran-2(1H)-one
Synonyms: 17b-hydroxy-17a-methyl-2-oxa-5a-androstan-3-one; dodecahydro-3-hydroxy-6-(hydroxymethyl)-3,3a,6-trimethyl-1H-benz[e]indene-7-acetic acid d-lactone
Trademarks: Anavar (Searle); Lonavar (Searle); Provitar (Clin-Comar-Byla); Vasorome (Kowa)
Molecular Formula: C19H30O3
Molecular Weight: 306.44
Percent Composition: C 74.47%, H 9.87%, O 15.66%
Literature References: Prepn: R. Pappo, C. J. Jung, Tetrahedron Lett. 9, 365 (1962); R. Pappo, US 3128283 (1964 to Searle).
Properties: Crystals, mp 235-238°. [a]D25 -23° (c = approx 1% in chloroform).
Melting point: mp 235-238°
Optical Rotation: [a]D25 -23° (c = approx 1% in chloroform)
NOTE: This is a controlled substance (anabolic steroid): 21 CFR, 1308.13, as defined in 1300.01.
Therap-Cat: Androgen.
Keywords: Androgen.