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141109-17-3

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141109-17-3 Usage

General Description

D(+)-Chloro phenyl glycine methyl ester is a chemical compound that belongs to the family of amino acid derivatives. It is a crystalline solid with a molecular formula of C9H10ClNO2 and a molecular weight of 201.63 g/mol. D(+)-Chloro phenyl glycine methyl ester is commonly used as a building block in the synthesis of various pharmaceuticals and agrochemicals due to its ability to serve as a chiral source of glycine. It is also utilized in the production of certain dyes and pigments. D(+)-Chloro phenyl glycine methyl ester is considered to be stable under normal conditions, but it may react with strong oxidizing agents. It is important to handle and store this chemical in accordance with proper safety precautions to prevent any potential hazards.

Check Digit Verification of cas no

The CAS Registry Mumber 141109-17-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,1,1,0 and 9 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 141109-17:
(8*1)+(7*4)+(6*1)+(5*1)+(4*0)+(3*9)+(2*1)+(1*7)=83
83 % 10 = 3
So 141109-17-3 is a valid CAS Registry Number.

141109-17-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name (+/-)-2-chlorophenylglycine methyl ester hydrochloride

1.2 Other means of identification

Product number -
Other names D(+)-CHLORO PHENYL GLYCINE METHYL 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:141109-17-3 SDS

141109-17-3Relevant articles and documents

Isotopically Directed Symmetry Breaking and Enantioenrichment in Attrition-Enhanced Deracemization

Blackmond, Donna G.,Houk, K. N.,Murray, James I.,Richardson, Paul F.,Sanders, Jacob N.

supporting information, (2020/03/10)

The evolution of homochirality via attrition-enhanced deracemization (AED) of enantiomorphic solids is carried out using molecules that differ only in the isotopic composition of a phenyl group positioned remote from the chiral center. Enantioenrichment c

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