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CAS

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537718-14-2

Androst-5-en-17-one, 3,7,11-tris[(methoxycarbonyl)oxy]-, (3beta,7beta,11alpha)- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

537718-14-2

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537718-14-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 537718-14-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,3,7,7,1 and 8 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 537718-14:
(8*5)+(7*3)+(6*7)+(5*7)+(4*1)+(3*8)+(2*1)+(1*4)=172
172 % 10 = 2
So 537718-14-2 is a valid CAS Registry Number.

537718-14-2SDS

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 [(3S,7R,8S,9S,10R,11R,13S,14S)-3,7-bis(methoxycarbonyloxy)-10,13-dimethyl-17-oxo-1,2,3,4,7,8,9,11,12,14,15,16-dodecahydrocyclopenta[a]phenanthren-11-yl] methyl carbonate

1.2 Other means of identification

Product number -
Other names -

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:537718-14-2 SDS

537718-14-2Downstream Products

537718-14-2Relevant articles and documents

Processes for preparing C-7 substituted steroids

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Page/Page column 4; 10, (2008/06/13)

This invention relates to processes for the preparation of novel 7-carboxy substituted steroid compounds of Formula I,

New process for the preparation of methyl carbonates

Wuts, Peter G. M.,Ashford, Scott W.,Anderson, Andrew M.,Atkins, Joseph R.

, p. 1483 - 1485 (2007/10/03)

(Matrix presented) The methyl carbonate of HOBt was developed for the conversion of alcohols to carbonates. This method is superior to the use of methyl chloroformate or methyl pyrocarbonate, especially with more hindered alcohols. The reagent is a stable solid that is easily prepared on a multigram scale.

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