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

537718-07-3

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537718-07-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 537718-07-3 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, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 537718-07:
(8*5)+(7*3)+(6*7)+(5*7)+(4*1)+(3*8)+(2*0)+(1*7)=173
173 % 10 = 3
So 537718-07-3 is a valid CAS Registry Number.

537718-07-3SDS

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 3β,7β,11α-trihydroxy-5-androsten-17-one

1.2 Other means of identification

Product number -
Other names 5-androsten-3β,7β,11α-triol-17-one

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:537718-07-3 SDS

537718-07-3Relevant academic research and scientific papers

A chemobiological synthesis of eplerenone

Wuts, Peter G. M.,Anderson, Andrew M.,Ashford, Scott W.,Goble, Michael P.,White, Michael J.,Beck, Doris,Gilbert, Ivan,Hrab

, p. 418 - 422 (2008/09/17)

This paper will describe an approach to the synthesis of eplerenone, which is being marketed for the treatment of hypertension. The synthesis begins with DHEA available from wild yams and uses a combination of microbiological and chemical transformations to build eplerenone. Georg Thieme Verlag Stuttgart.

Processes for preparing C-7 substituted steroids

-

Page/Page column 9, (2008/06/13)

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

Microbial method for hydrolysis and oxidation of androst-5-ene and pregn-5-ene steroid esters

-

, (2008/06/13)

A microbial method for hydrolysis and oxidation of androst-5-ene and pregn-5-ene steroid esters is disclosed.

Processes for preparing 7-carboxy substituted steroids

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Page 16, (2008/06/13)

This invention relates to processes for the preparation of 7-carboxy substituted steroid compounds of Formula I, wherein R1 is selected from H or COR4; R4 is C1-C6 alkyl or C1-C6 alkoxy; R3 is C1-C6 alkyl; Z1 is —CH2— or wherein O—COR4 is in the α configuration; Z2 is —CH—; or Z1 and Z2 may be taken together to form a carbon-carbon double bond; Q is These intermediates are useful in the preparation of 7-carboxy substituted steroid compounds, and particularly, the invention is directed to novel and advantageous methods for the preparation of 9,11-α-epoxy-17-α-hydroxy-3-oxopregn-4-ene-α-7-21-dicarboxylic acid, γ-lactone, methyl ester (eplerenone; epoxymexrenone).

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