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Benzamide, 2-chloro-N-[2-[4-(phenylmethyl)-1-piperazinyl]ethyl]- is a complex organic compound with the chemical formula C20H24ClN3O. It is a derivative of benzamide, featuring a 2-chloro substituent and a 2-[4-(phenylmethyl)-1-piperazinyl]ethyl chain attached to the nitrogen atom. Benzamide, 2-chloro-N-[2-[4-(phenylmethyl)-1-piperazinyl]ethyl]- is known for its potential applications in pharmaceutical research, particularly as a building block for the synthesis of various drugs. Its structure includes a benzene ring, an amide group, a chloro substituent, and a piperazine ring, which together contribute to its unique chemical properties and potential therapeutic effects.

100221-91-8

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100221-91-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 100221-91-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,2,2 and 1 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 100221-91:
(8*1)+(7*0)+(6*0)+(5*2)+(4*2)+(3*1)+(2*9)+(1*1)=48
48 % 10 = 8
So 100221-91-8 is a valid CAS Registry Number.

100221-91-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name N-[2-(4-Benzyl-piperazin-1-yl)-ethyl]-2-chloro-benzamide

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

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More Details:100221-91-8 SDS

100221-91-8Downstream Products

100221-91-8Relevant academic research and scientific papers

Synthesis, biological evaluation, and quantitative structure. A new class of potent H1 antagonists

Saxena,Agarwal,Patnaik,Saxena

, p. 2970 - 2976 (2007/10/02)

Some [β-(Aroylamino)ethyl]piperazines and -piperidines and [2-[(Arylamino)carbonyl]ethyl]piperazines, -piperidines, -pyrazinopyridoindoles, and -pyrazinoisoquinolines have been synthesized and their H1-antagonistic activity studied in isolated guinea pig

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