ChemicalBook >> CAS DataBase List >>(8S,9S,13S,14S,17S)-17-hydroxy-13-methyl-2,4,6,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-one

(8S,9S,13S,14S,17S)-17-hydroxy-13-methyl-2,4,6,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-one

CAS No.
1089-78-7
Chemical Name:
(8S,9S,13S,14S,17S)-17-hydroxy-13-methyl-2,4,6,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-one
Synonyms
NSC 37320;Prenortestosterone;17β-Hydroxyestr-5(10)-en-3-one;Estr-5(10)-en-3-one, 17-hydroxy-, (17β)-;17β-Hydroxy-19-norandrost-5(10)-en-3-one;(8R,9S,13S,14S,17S)-17-hydroxy-13-methyl-2,4,6,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-one;(8S,9S,13S,14S,17S)-17-hydroxy-13-methyl-2,4,6,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-one
CBNumber:
CB01465802
Molecular Formula:
C18H26O2
Molecular Weight:
274.4
MDL Number:
MOL File:
1089-78-7.mol
Last updated:2023-05-15 10:44:02

(8S,9S,13S,14S,17S)-17-hydroxy-13-methyl-2,4,6,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-one Properties

Melting point 199.8-201 °C (decomp)(Solv: ethyl acetate (141-78-6))
Boiling point 428.7±45.0 °C(Predicted)
Density 1.14±0.1 g/cm3(Predicted)
vapor pressure 0.001Pa at 20℃
solubility Chloroform (Slightly), Ethanol (Slightly, Sonicated)
pka 15.06±0.40(Predicted)
form Solid
color White to Off-White
Water Solubility 3.1mg/L at 20℃
LogP 3.1
FDA UNII 99T8YP2W04

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS08
Signal word  Danger
Hazard statements  H351-H362-H360
Precautionary statements  P201-P260-P263-P264-P270-P308+P313-P201-P202-P281-P308+P313-P405-P501

(8S,9S,13S,14S,17S)-17-hydroxy-13-methyl-2,4,6,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-one Chemical Properties,Uses,Production

Uses

Testosterone (T155000) derivative. Inhibits estrogen biosynthesis. A steroid ligand for the cytosol androgen receptor (AR) of rat prostate.

Definition

ChEBI: 17beta-hydroxyestr-5(10)-en-3-one is a 3-oxo steroid that is estr-5(10)-ene substituted by an oxo group at position 3 and a beta-hydroxy group at position 17. It is a 3-oxo steroid and a 17beta-hydroxy steroid. It derives from a hydride of an estrane.

(8S,9S,13S,14S,17S)-17-hydroxy-13-methyl-2,4,6,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-one Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 10)Suppliers
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View Lastest Price from (8S,9S,13S,14S,17S)-17-hydroxy-13-methyl-2,4,6,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-one manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
8S,9S,13S,14S,17S)-17-hydroxy-13-methyl-2,4,6,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-one pictures 2019-07-06 8S,9S,13S,14S,17S)-17-hydroxy-13-methyl-2,4,6,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-one
1089-78-7
US $7.00 / KG 1KG 99% 100KG Career Henan Chemical Co
(8S,9S,13S,14S,17S)-17-hydroxy-13-methyl-2,4,6,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-one (8R,9S,13S,14S,17S)-17-hydroxy-13-methyl-2,4,6,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-one 17β-Hydroxy-19-norandrost-5(10)-en-3-one 17β-Hydroxyestr-5(10)-en-3-one NSC 37320 Prenortestosterone Estr-5(10)-en-3-one, 17-hydroxy-, (17β)- 1089-78-7 Intermediates & Fine Chemicals Pharmaceuticals Steroids