Home > Name List By other > (5R,8S,9S,10S,13S,14S)-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16, 17-tetradecahydro-1H-cyclopenta[a]phenanthrene Germany

CAS No 438-22-2 , (5R,8S,9S,10S,13S,14S)-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,
17-tetradecahydro-1H-cyclopenta[a]phenanthrene Search by region : Germany

  • Name: (5R,8S,9S,10S,13S,14S)-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,
    17-tetradecahydro-1H-cyclopenta[a]phenanthrene
  • Synonyms: Androstane; (5.alpha.)-; 438-22-2;5alpha-Androstane;(5R,8S,9S,10S,13S,14S)-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,
    17-tetradecahydro-1H-cyclopenta[a]phenanthrene; Etioallocholane; Aetioallocholane; 5.alpha.-Androstane; 5a-androstane; Aetioallocholan;
  • CAS Registry Number:
  • Transport: UN 1593 6.1/PG 3
  • Flash Point: 145.9°C
  • Boiling Point: 336°Cat760mmHg
  • Density: 0.95g/cm3
  • Refractive index: 1.508
  • Safety Statements: Hazard Codes TRisk Statements 45-23/24/25-36/37/38-43-63Safety Statements 53-23-24/25-36/37RIDADR UN 1593 6.1/PG 3WGK Germany 3
  • Hazard Symbols: T: Toxic;
  • Flash Point: 145.9°C
  • EINECS: 207-116-2
  • Molecular Weight: 260.45738
  • InchiKey: QZLYKIGBANMMBK-UGCZWRCOSA-N
  • InChI: InChI=1S/C19H32/c1-18-11-5-7-16(18)15-9-8-14-6-3-4-12-19(14,
    2)17(15)10-13-18/h14-17H,3-13H2,1-2H3/t14-,15+,16+,17+,18+,19+/m1/s1
  • Risk Statements: 45-23/24/25-36/37/38-43-63
  • Molecular Formula: C19H32
  • Molecular Structure:CAS No:438-22-2 (5R,8S,9S,10S,13S,14S)-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,<br />17-tetradecahydro-1H-cyclopenta[a]phenanthrene

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438-22-2 0674.19-100-IO 5ALPHA(H)-ANDROSTANE

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438-22-2 5-alpha-Androstane

  • 5-alpha-Androstane
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References of (5R,8S,9S,10S,13S,14S)-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,
17-tetradecahydro-1H-cyclopenta[a]phenanthrene
Title: Androstane
CAS Registry Number: 438-22-2
CAS Name: (5a)-Androstane
Synonyms: etioallocholane
Molecular Formula: C19H32
Molecular Weight: 260.46
Percent Composition: C 87.62%, H 12.38%
Literature References: From androstane-3,17-dione: Butenandt, Tscherning, Z. Physiol. Chem. 229, 185 (1934). From androstane-3,17-diol: Steiger, Reichstein, Helv. Chim. Acta 20, 817 (1937). From D16-androstene: Prelog et al., ibid. 27, 66 (1944).
Properties: Leaflets from acetone-methanol, mp 50-50.5°. Sublimes at 60° and 0.003 mm Hg. [a]D16 +2° (c = 1.2 in chloroform). Sol in acetone, alc, methanol, ether, petr ether, chloroform.
Melting point: mp 50-50.5°
Optical Rotation: [a]D16 +2° (c = 1.2 in chloroform)
 
Derivative Type: 17-Amino-HCl
Properties: Dec 345°: Marker, J. Am. Chem. Soc. 58, 480 (1936).