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Ethanone, 2-[(3,4-dichlorophenyl)methylamino]-1-[4-(phenylsulfonyl)-2-(1-pyrrolidinylmethyl)-1-piperazinyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1053179-66-0

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1053179-66-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1053179-66-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,5,3,1,7 and 9 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1053179-66:
(9*1)+(8*0)+(7*5)+(6*3)+(5*1)+(4*7)+(3*9)+(2*6)+(1*6)=140
140 % 10 = 0
So 1053179-66-0 is a valid CAS Registry Number.

1053179-66-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[(3,4-Dichlorophenyl)(methyl)amino]-1-[4-(phenylsulfonyl)-2-(1- pyrrolidinylmethyl)-1-piperazinyl]ethanone

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:1053179-66-0 SDS

1053179-66-0Downstream Products

1053179-66-0Relevant articles and documents

Aminomethylpiperazines as selective urotensin antagonists

Hilfiker, Mark A.,Zhang, Daohua,Dowdell, Sarah E.,Goodman, Krista B.,McAtee, John J.,Dodson, Jason W.,Viet, Andrew Q.,Wang, Gren Z.,Sehon, Clark A.,Behm, David J.,Wu, Zining,Carballo, Luz H.,Douglas, Stephen A.,Neeb, Michael J.

scheme or table, p. 4470 - 4473 (2009/04/06)

Aminomethylpiperazines, reported previously as being κ-opioid receptor agonists, were identified as lead compounds in the development of selective urotensin receptor antagonists. Optimized substitution of the piperazine moiety has provided high affinity u

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