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51063-99-1

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51063-99-1 Usage

General Description

ETHYL(R)(+)-2-BROMO-PROPANOATE is a chemical compound with the molecular formula C5H9BrO2. It is an ester, specifically the ethyl ester of (R)-2-bromo-propanoic acid. ETHYL(R)(+)-2-BROMO-PROPANOATE is often used in organic synthesis as a reagent for creating various pharmaceuticals and other organic compounds. It is a colorless liquid with a fruity, sweet odor, and it is known to be flammable and hazardous if not handled properly. Its main applications include its use in the pharmaceutical industry and as a chemical intermediate in the production of other organic compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 51063-99-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,0,6 and 3 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 51063-99:
(7*5)+(6*1)+(5*0)+(4*6)+(3*3)+(2*9)+(1*9)=101
101 % 10 = 1
So 51063-99-1 is a valid CAS Registry Number.

51063-99-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (R)-ethyl 2-bromopropanoate

1.2 Other means of identification

Product number -
Other names (R)-(+)-ethyl 2-brmopropionate

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:51063-99-1 SDS

51063-99-1Relevant articles and documents

Enantiodiscrimination of racemic electrophiles by diketopiperazine enolates: asymmetric synthesis of methyl 2-amino-3-aryl-butanoates and 3-methyl-aspartates

Bull, Steven D.,Davies, Stephen G.,Epstein, Simon W.,Garner, A. Christopher,Mujtaba, Nadeam,Roberts, Paul M.,Savory, Edward D.,Smith, Andrew D.,Tamayo, Juan A.,Watkin, David J.

, p. 7911 - 7925 (2007/10/03)

Enolates of (S)-N,N′-bis-(p-methoxybenzyl)-3-iso-propylpiperazine-2,5-dione exhibit high levels of enantiodiscrimination in alkylations with (RS)-1-aryl-1-bromoethanes and (RS)-2-bromoesters, affording substituted diketopiperazines containing two new stereogenic centres in high de. Deprotection and hydrolysis of the resultant substituted diketopiperazines provides a route to the asymmetric synthesis of homochiral methyl 2-amino-3-aryl-butanoates and 3-methyl-aspartates in high de and ee.

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