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Benzenebutanoic acid, -gamma--(acetyloxy)--ba--methyl-, (-ba-S,-gamma-R)- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

853759-96-3

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853759-96-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 853759-96-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,3,7,5 and 9 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 853759-96:
(8*8)+(7*5)+(6*3)+(5*7)+(4*5)+(3*9)+(2*9)+(1*6)=223
223 % 10 = 3
So 853759-96-3 is a valid CAS Registry Number.

853759-96-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name (3S,4R)-4-acetoxy-3-methyl-4-phenylbutyric acid

1.2 Other means of identification

Product number -
Other names (3S,4R)-4-Acetoxy-3-methyl-4-phenyl-butyric acid

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:853759-96-3 SDS

853759-96-3Downstream Products

853759-96-3Relevant academic research and scientific papers

A concise synthetic route to optically active cis-β,γ- disubstituted-γ-butyrolactones via tandem Michael-MPV reaction: New total synthesis of (-)-cis-whisky lactone and (-)-cis-cognac lactone

Ozeki, Minoru,Hashimoto, Daisuke,Nishide, Kiyoharu,Kajimoto, Tetsuya,Node, Manabu

, p. 1663 - 1671 (2007/10/03)

Optically active cis-β,γ-disubstituted-γ-butyrolactones, for example, cis-whisky lactone and cis-cognac lactone, were readily synthesized by using tandem Michael-Meerwein-Ponndorf-Verley reactions that employed (-)-10-mercapto-isoborneol as a chiral template in the key step.

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