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Benzeneacetic acid, 3-[2-[(2-chloroacetyl)amino]-2-methylpropyl]-, ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

921598-15-4

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921598-15-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 921598-15-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,2,1,5,9 and 8 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 921598-15:
(8*9)+(7*2)+(6*1)+(5*5)+(4*9)+(3*8)+(2*1)+(1*5)=184
184 % 10 = 4
So 921598-15-4 is a valid CAS Registry Number.

921598-15-4SDS

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 ethyl 2-{3-[2-(2-chloroacetamido)-2-methylpropyl]phenyl}acetate

1.2 Other means of identification

Product number -
Other names {3-[2-(2-chloro-acetylamino)-2-methyl-propyl]-phenyl}-acetic acid ethyl 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:921598-15-4 SDS

921598-15-4Relevant academic research and scientific papers

Enzymatic desymmetrization route to ethyl [3-(2-amino-2-methylpropyl) phenyl]acetate

De Koning, Pieter D.,Gladwell, Iain R.,Morrison, Natalie A.,Moses, Ian B.,Panesar, Maninder S.,Pettman, Alan J.,Thomson, Nicholas M.,Yazbeck, Daniel R.

, p. 871 - 875 (2012/06/18)

An efficient process to ethyl [3-(2-amino-2-methylpropyl)phenyl]acetate 6 has been developed. Key steps include a novel enzymatic desymmetrization of diester 2 and a Ritter reaction between alcohol 4 and chloroacetonitrile, followed by chemoselective deprotection with thiourea.

PROCESS FOR THE PREPARATION OF SULFONAMIDE DERIVATIVES

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Page/Page column 33-34, (2010/11/25)

The invention relates to a process for the preparation of compounds of formula (I) wherein Q1 is a group selected from formulae (II and (III) and a group *-NR6 -Q2-A or, if appropriate, their pharmaceutically acceptable sa

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