Home > Name List By other > (8S,9S,10R,13S,14S,17S)-17-(2-hydroxyacetyl)-10,13-dimethyl-1,2,6,7,8,9, 11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthre... Germany

CAS No 64-85-7 , (8S,9S,10R,13S,14S,17S)-17-(2-hydroxyacetyl)-10,13-dimethyl-1,2,6,7,8,9,
11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one Search by region : Germany

  • Name: (8S,9S,10R,13S,14S,17S)-17-(2-hydroxyacetyl)-10,13-dimethyl-1,2,6,7,8,9,
    11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one
  • Synonyms: 11-Desoxycorticosterone; Deoxycorticosterone; Cortexone;(8S,9S,10R,13S,14S,17S)-17-(2-hydroxyacetyl)-10,13-dimethyl-1,2,6,7,8,9,
    11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one; 21-Hydroxyprogesterone; 11-Deoxycorticosterone;Desoxycortone; Deoxycortone;
  • CAS Registry Number:
  • Transport: UN 2811
  • Melting Point: 138-144 ºC
  • Density: 1.15 g/cm3
  • Refractive index: 1.559
  • Alpha: 184 º (C=1, C2H5OH)
  • Safety Statements: R40;R48
  • Hazard Symbols: Xn: Harmful;
  • EINECS: 200-596-4
  • Molecular Weight: 330.4611
  • InchiKey: ZESRJSPZRDMNHY-YFWFAHHUSA-N
  • InChI: InChI=1S/C21H30O3/c1-20-9-7-14(23)11-13(20)3-4-15-16-5-6-18(19(24)12-22)
    21(16,2)10-8-17(15)20/h11,15-18,22H,3-10,12H2,1-2H3/t15-,16-,17-,18+,
    20-,21-/m0/s1
  • Risk Statements: S22;S24/25
  • Molecular Formula: C21H30O3
  • Molecular Structure:CAS No:64-85-7 (8S,9S,10R,13S,14S,17S)-17-(2-hydroxyacetyl)-10,13-dimethyl-1,2,6,7,8,9,<br />11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one

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64-85-7 Desoxycorticosterone

  • Desoxycorticosterone
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References of (8S,9S,10R,13S,14S,17S)-17-(2-hydroxyacetyl)-10,13-dimethyl-1,2,6,7,8,9,
11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one
Title: Deoxycorticosterone
CAS Registry Number: 64-85-7
CAS Name: 21-Hydroxypregn-4-ene-3,20-dione
Synonyms: 4-pregnen-21-ol-3,20-dione; 21-hydroxyprogesterone; desoxycorticosterone; 11-deoxycorticosterone; cortexone; desoxycortone; Kendall's desoxy compound B; Reichstein's substance Q
Molecular Formula: C21H30O3
Molecular Weight: 330.46
Percent Composition: C 76.33%, H 9.15%, O 14.52%
Literature References: Occurs in adrenal cortex: Reichstein, von Euw, Helv. Chim. Acta 21, 1197 (1938); Steiger, Reichstein, ibid. 20, 1164 (1937). Numerous prepns from other steroids: Schindler et al., ibid. 24, 371 (1941); Reichstein, DE 875353 (1953 to Schering); Bockmühl et al., DE 871153 (1953 to Hoechst); Wettstein et al., US 2778776 (1957 to Ciba); NL 89575 (1958 to Organon); Kaspar et al., DE 1028572 (1958 to Schering). Isoln from the prothoracal glands of the water beetle, Dytiscus marginalis: Schildknecht et al., Angew. Chem. 78, 392 (1966).
Properties: Plates from ether, mp 141-142°. [a]D22 +178° (alc). uv max: 240 nm. Freely sol in alcohol, acetone.
Melting point: mp 141-142°
Optical Rotation: [a]D22 +178° (alc)
Absorption maximum: uv max: 240 nm
 
Derivative Type: Acetate see Deoxycortiscosterone Acetate
 
Derivative Type: Tetraacetyl-b-D-glucoside
Molecular Formula: C35H48O12
Molecular Weight: 660.75
Percent Composition: C 63.62%, H 7.32%, O 29.06%
Properties: Clusters of needles from 50% alc, mp 176-176.5°. [a]D24 +80° (c = 0.515 in chloroform). Believed to occur in nature in this glycosidic form: Johnson, J. Am. Chem. Soc. 63, 3238 (1941).
Melting point: mp 176-176.5°
Optical Rotation: [a]D24 +80° (c = 0.515 in chloroform)
 
Therap-Cat: Mineralocorticoid.
Keywords: Mineralocorticoid.