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6-hydroxycholest-4-en-3-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

69853-71-0

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69853-71-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 69853-71-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,8,5 and 3 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 69853-71:
(7*6)+(6*9)+(5*8)+(4*5)+(3*3)+(2*7)+(1*1)=180
180 % 10 = 0
So 69853-71-0 is a valid CAS Registry Number.

69853-71-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

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

1.2 Other means of identification

Product number -
Other names Cholest-4-en-3-one,6-hydroxy

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:69853-71-0 SDS

69853-71-0Downstream Products

69853-71-0Relevant academic research and scientific papers

Anti-obesity agents

-

, (2008/06/13)

Disclosed are anti-obesity agents comprising 3-ketosteroidal compounds as defined in the specification. The present invention also discloses pharmaceutical compositions and use of these compounds in the prevention and treatment of obesity.

Allylic Hydroperoxides Formed by Singlet Oxygenation of Cholest-5-en-3-one

Dang, Hai-Shan,Davies, Alwyn G.,Schiesser, Carl H.

, p. 789 - 794 (2007/10/02)

Cholest-5-en-3-one (I) reacts with singlet oxygen to give the hemiperketal (II) (ca. 55percent), the epimeric 6β- and 6α-hydroperoxides (III) and (IV) (ca. 30 and 8percent respectively), and the dione (V) (ca 7percent).The hemiperketal (II) does not undergo an allylic rearrangement in solution, but the hydroperoxides (III) and (IV) epimerise by a radical chain mechanism. .Stereochemical problems connected with this system have been probed by carrying out parallel experiments and molecular mechanics calculations on the corresponding derivatives of methyloctahydronaphthalenone as model compounds.

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