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Benzamide, N-(2-chloroethyl)-3-methoxy- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

161194-75-8

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161194-75-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 161194-75-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,1,1,9 and 4 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 161194-75:
(8*1)+(7*6)+(6*1)+(5*1)+(4*9)+(3*4)+(2*7)+(1*5)=128
128 % 10 = 8
So 161194-75-8 is a valid CAS Registry Number.

161194-75-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(2-chloroethyl)-3-methoxybenzamide

1.2 Other means of identification

Product number -
Other names -

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:161194-75-8 SDS

161194-75-8Relevant academic research and scientific papers

N-[2-[4-(4-chlorophenyl)piperazin-1-yl]ethyl]-3-methoxybenzamide: A potent and selective dopamine D4 ligand

Perrone,Berardi,Colabufo,Leopoldo,Tortorella

, p. 4903 - 4909 (2007/10/03)

A series of new 1-aryl-4-alkylpiperazines containing a terminal benzamide fragment or a tetralin-1-yl nucleus on the alkyl chain were synthesized and tested for binding at cloned human dopamine D4 and D2 receptor subtypes. A SAFIR (s

The Use of 2-Oxazolidinone as a Latent Aziridine Equivalent. I. A Facile Method for the Preparation of 2-Substituted Oxazolines

Poindexter, Graham S.

, p. 1431 - 1433 (2007/10/02)

Ring-opening reaction of 2-oxazolidinone with acid chlorides followed by treatment with aqueous sodium hydroxide yields 2-substituted oxazolines.

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