Home > Name List By other > (8R,9S,13S,14S,17R)-13-methyl-6,7,8,9,11,12,14,15,16, 17-decahydrocyclopenta[a]phenanthrene-3,17-diol Germany

CAS No 57-91-0 , (8R,9S,13S,14S,17R)-13-methyl-6,7,8,9,11,12,14,15,16,
17-decahydrocyclopenta[a]phenanthrene-3,17-diol Search by region : Germany

  • Name: (8R,9S,13S,14S,17R)-13-methyl-6,7,8,9,11,12,14,15,16,
    17-decahydrocyclopenta[a]phenanthrene-3,17-diol
  • Synonyms: alpha-Estradiol;(8R,9S,13S,14S,17R)-13-methyl-6,7,8,9,11,12,14,15,16,
    17-decahydrocyclopenta[a]phenanthrene-3,17-diol; 17alpha-Estradiol; Epiestradial; Estradiol-17alpha; 3,17-Dihydroxyestratriene; Alfatradiol;Epiestradiol; 57-91-0; 17-alpha-Estradiol;
  • CAS Registry Number:
  • Transport: UN 2811
  • Density: 1.17 g/cm3
  • Refractive index: 1.599
  • Water Solubility: ethanol: 50 mg/mL, clear, colorless
  • Safety Statements: Experimental reproductive effects. Questionable carcinogen with experimental tumorigenic data. Human mutation data reported. When heated to decomposition it emits acrid smoke and irritating fumes. A steroid. See also ESTRADIOL.
  • Hazard Symbols: Xn: Harmful;
  • EINECS: 200-354-8
  • Molecular Weight: 272.38196
  • InchiKey: VOXZDWNPVJITMN-SFFUCWETSA-N
  • InChI: InChI=1S/C18H24O2/c1-18-9-8-14-13-5-3-12(19)10-11(13)2-4-15(14)16(18)6-
    7-17(18)20/h3,5,10,14-17,19-20H,2,4,6-9H2,1H3/t14-,15-,16+,17-,18+/m1/s1
  • Risk Statements: R40;R48
  • Molecular Formula: C18H24O2
  • Molecular Structure:CAS No:57-91-0 (8R,9S,13S,14S,17R)-13-methyl-6,7,8,9,11,12,14,15,16,<br />17-decahydrocyclopenta[a]phenanthrene-3,17-diol

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57-91-0 17-alpha-Estradiol

  • 17-alpha-Estradiol
  • Germany CHEMOS GmbH [Manufacturer]
  • Tel: 0049 9402/9336 0
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  • Address: CHEMOS GmbH
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References of (8R,9S,13S,14S,17R)-13-methyl-6,7,8,9,11,12,14,15,16,
17-decahydrocyclopenta[a]phenanthrene-3,17-diol
Title: a-Estradiol
CAS Registry Number: 57-91-0
CAS Name: (17a)-Estra-1,3,5(10)-triene-3,17-diol
Synonyms: 1,3,5-estratriene-3,17a-diol; 3,17-dihydroxyestratriene
Molecular Formula: C18H24O2
Molecular Weight: 272.38
Percent Composition: C 79.37%, H 8.88%, O 11.75%
Literature References: Has been isolated from pregnancy urine of mares. Prepn from b-estradiol by inversion of the hydroxyl group at C-17 after tosylation: Allais, Hoffmann, US 2835681 (1958).
Properties: Needles with ?H2O from 80% alcohol, mp 220-223°. [a]D20 +53 to +56° (c = 0.9 in dioxane). Not precipitated by digitonin (in 80% alcoholic soln). Soluble in alcohol, acetone, aq alkalies. One gram dissolves in more than 100 ml of boiling benzene. Slightly sol in ether, chloroform. Insol in water, aq dil acids.
Melting point: mp 220-223°
Optical Rotation: [a]D20 +53 to +56° (c = 0.9 in dioxane)
 
Derivative Type: Diacetate
Molecular Formula: C22H28O4
Molecular Weight: 356.46
Percent Composition: C 74.13%, H 7.92%, O 17.95%
Properties: mp 140-142°.
Melting point: mp 140-142°
 
Derivative Type: 3-Benzoate
Molecular Formula: C25H28O3
Molecular Weight: 376.49
Percent Composition: C 79.75%, H 7.50%, O 12.75%
Properties: mp 156-157°; also reported as polymorphous: I, mp 63°; II, mp 153°; III, mp 158°.
Melting point: mp 156-157°; also reported as polymorphous: I, mp 63°; II, mp 153°; III, mp 158°