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Benzeneacetic acid, a-bromo-, octyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

530091-82-8

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530091-82-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 530091-82-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,3,0,0,9 and 1 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 530091-82:
(8*5)+(7*3)+(6*0)+(5*0)+(4*9)+(3*1)+(2*8)+(1*2)=118
118 % 10 = 8
So 530091-82-8 is a valid CAS Registry Number.

530091-82-8SDS

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 (+/-)-2-bromo-2-phenylacetic acid octyl ester

1.2 Other means of identification

Product number -
Other names Bromo-phenyl-acetic acid octyl ester

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:530091-82-8 SDS

530091-82-8Relevant articles and documents

Lipase-catalyzed enantioselective transesterification toward esters of 2-bromo-tolylacetic acids

Guieysse, David,Salagnad, Christophe,Monsan, Pierre,Remaud-Simeon, Magali

, p. 317 - 323 (2007/10/03)

Lipases from Candida antarctica, Pseudomonas cepacia and Rhizomucor miehei were tested in the resolution of seven racemic substrates belonging to the (RS)-2-bromo tolyl acetate ester category, but differing either in the position of the methyl substituent on the acyl part of the aromatic ring, or in the structure of the alkyl group. Lipase-catalyzed kinetic resolution via transesterification reaction between the ester and octanol in octane revealed that, of the three enzymes tested, P. cepacia lipase is the most efficient for resolution of the various racemates, with R-enantiopreference. In addition, the position of the methyl substituent was found to play a key role in governing the enantioselectivity of the reaction. Using P. cepacia lipase and 2-bromo-m/p-tolyl- or 2-bromophenylacetic acid esters E-values of 6.

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