Home > Name List By other > [(8R,9S,10R,13S,14S,17R)-17-acetyl-6-chloro-10,13-dimethyl-3-oxo-9,11, 12,14,15,16-hexahydro-8H-cyclopenta[a]phenanthren-17-y... China

CAS No 13698-49-2 , [(8R,9S,10R,13S,14S,17R)-17-acetyl-6-chloro-10,13-dimethyl-3-oxo-9,11,
12,14,15,16-hexahydro-8H-cyclopenta[a]phenanthren-17-yl] acetate Search by region : China

  • Name: [(8R,9S,10R,13S,14S,17R)-17-acetyl-6-chloro-10,13-dimethyl-3-oxo-9,11,
    12,14,15,16-hexahydro-8H-cyclopenta[a]phenanthren-17-yl] acetate
  • Synonyms: Delmadinone acetate [USAN]; 13698-49-2; RS-1301;DELMADINONE ACETATE;[(8R,9S,10R,13S,14S,17R)-17-acetyl-6-chloro-10,13-dimethyl-3-oxo-9,11,
    12,14,15,16-hexahydro-8H-cyclopenta[a]phenanthren-17-yl] acetate; RS 1301; Tardastrex; Delmadinone acetate (USAN);
  • CAS Registry Number:
  • Density: 1.25 g/cm3
  • Refractive index: 1.576
  • EINECS: 237-219-8
  • Molecular Weight: 402.91108
  • InchiKey: CGBCCZZJVKUAMX-DFXBJWIESA-N
  • InChI: InChI=1S/C23H27ClO4/c1-13(25)23(28-14(2)26)10-7-18-16-12-20(24)19-11-15
    (27)5-8-21(19,3)17(16)6-9-22(18,23)4/h5,8,11-12,16-18H,6-7,9-10H2,
    1-4H3/t16-,17+,18+,21-,22+,23+/m1/s1
  • Molecular Formula: C23H27ClO4
  • Molecular Structure:CAS No:13698-49-2 [(8R,9S,10R,13S,14S,17R)-17-acetyl-6-chloro-10,13-dimethyl-3-oxo-9,11,<br />12,14,15,16-hexahydro-8H-cyclopenta[a]phenanthren-17-yl] acetate

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References of [(8R,9S,10R,13S,14S,17R)-17-acetyl-6-chloro-10,13-dimethyl-3-oxo-9,11,
12,14,15,16-hexahydro-8H-cyclopenta[a]phenanthren-17-yl] acetate
Title: Delmadinone Acetate
CAS Registry Number: 13698-49-2
CAS Name: 17-(Acetyloxy)-6-chloropregna-1,4,6-triene-3,20-dione
Synonyms: 6-chloro-17-hydroxypregna-1,4,6-triene-3,20-dione acetate; 1,6-bisdehydro-6-chloro-17a-acetoxyprogesterone; D1-chlormadinone acetate
Manufacturers' Codes: RS-1301
Trademarks: Delminal (Rh>e-M?ieux); Estrex (Syntex); Tardastrex (Gruntex); Tarden (Veterinaria); Zenadrex (Veterinaria)
Molecular Formula: C23H27ClO4
Molecular Weight: 402.91
Percent Composition: C 68.56%, H 6.75%, Cl 8.80%, O 15.88%
Literature References: Prepn: Ringold et al., J. Am. Chem. Soc. 81, 3485 (1959); GB 890315 (1962 to Upjohn), C.A. 57, 5996c (1962); 76, 14813y (1972); Campbell, Babcock, DE 1243682 (1967 to Upjohn), C.A. 67, 100343r (1967). Activity studies: Dorfman, Kincl, Steroids 1, 185 (1963); Weichert et al., Arzneim.-Forsch. 17, 1103 (1967); Gerber et al., J. Small Anim. Pract. 14, 151 (1973).
Properties: Crystals, mp 168-170°. [a]D -83° (chloroform). uv max (ethanol): 229, 258, 297 nm (log e 4.00, 4.00, 4.03).
Melting point: mp 168-170°
Optical Rotation: [a]D -83° (chloroform)
Absorption maximum: uv max (ethanol): 229, 258, 297 nm (log e 4.00, 4.00, 4.03)
Therap-Cat: Progestogen.
Therap-Cat-Vet: Progestogen.
Keywords: Progestogen.