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(6S,9S,10R,13S,14S,17S)-17-hydroxy-6,13-dimethyl-2,6,7,8,9,10,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-one is a complex organic compound with a unique molecular structure. It is characterized by its specific stereochemistry, with six chiral centers and a hydroxyl group at the 17th position. (6S,9S,10R,13S,14S,17S)-17-hydroxy-6,13-dimethyl-2,6,7,8,9,10,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-one belongs to the class of cyclopenta[a]phenanthrenes, which are known for their diverse biological activities and potential applications in various fields.

10529-96-1

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10529-96-1 Usage

Uses

Used in Anti-doping Applications:
(6S,9S,10R,13S,14S,17S)-17-hydroxy-6,13-dimethyl-2,6,7,8,9,10,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-one is used as a urinary biomarker to detect illegal steroid use. It is a metabolite of the anabolic steroid Boldenone, which is prohibited in sports due to its performance-enhancing effects. The detection of (6S,9S,10R,13S,14S,17S)-17-hydroxy-6,13-dimethyl-2,6,7,8,9,10,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-one in urine samples can provide evidence of the abuse of anabolic steroids, helping to maintain fair play and integrity in sports competitions.
Used in Pharmaceutical Research:
Due to its unique chemical structure and potential biological activities, (6S,9S,10R,13S,14S,17S)-17-hydroxy-6,13-dimethyl-2,6,7,8,9,10,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-one may be of interest to pharmaceutical researchers. It could be further investigated for its potential as a lead compound in the development of new drugs targeting various diseases and conditions. (6S,9S,10R,13S,14S,17S)-17-hydroxy-6,13-dimethyl-2,6,7,8,9,10,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-one's specific stereochemistry and functional groups may also be exploited to design novel drug candidates with improved efficacy and selectivity.
Used in Chemical Synthesis:
The complex structure of (6S,9S,10R,13S,14S,17S)-17-hydroxy-6,13-dimethyl-2,6,7,8,9,10,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-one makes it a valuable target for chemical synthesis. Researchers in the field of organic chemistry may be interested in developing new synthetic routes to (6S,9S,10R,13S,14S,17S)-17-hydroxy-6,13-dimethyl-2,6,7,8,9,10,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-one, as well as exploring its reactivity and potential applications in the synthesis of other complex organic molecules. This could lead to the discovery of new synthetic methods and the development of novel compounds with interesting properties and potential applications.

Check Digit Verification of cas no

The CAS Registry Mumber 10529-96-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,5,2 and 9 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 10529-96:
(7*1)+(6*0)+(5*5)+(4*2)+(3*9)+(2*9)+(1*6)=91
91 % 10 = 1
So 10529-96-1 is a valid CAS Registry Number.

10529-96-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (6S,9S,10R,13S,14S,17S)-17-hydroxy-6,13-dimethyl-2,6,7,8,9,10,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-one

1.2 Other means of identification

Product number -
Other names 4-Dihydroboldenone

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:10529-96-1 SDS

10529-96-1Downstream Products

10529-96-1Relevant academic research and scientific papers

HIO3 and I2O5: Mild and selective alternative reagents to IBX for the dehydrogenation of aldehydes and ketones

Nicolaou,Montagnon, Tamsyn,Baran, Phil S.

, p. 1386 - 1389 (2007/10/03)

Economic and convenient: Iodic acid (1) and iodine pentoxide (2) form complexes 3 and 4, respectively, with DMSO when heated at 80°C for 1 h. The complexes are efficient agents for the dehydrogenation of ketones and aldehydes at 45-65°C. X-ray crystallographic analysis (see picture) shows that the iodine pentoxide. DMSO complex 4 self-assembles into a remarkable helix in the solid state.

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