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371111-51-2

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371111-51-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 371111-51-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,7,1,1,1 and 1 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 371111-51:
(8*3)+(7*7)+(6*1)+(5*1)+(4*1)+(3*1)+(2*5)+(1*1)=102
102 % 10 = 2
So 371111-51-2 is a valid CAS Registry Number.

371111-51-2SDS

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 ethyl 5-(4-chlorophenyl)pentanoate

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:371111-51-2 SDS

371111-51-2Relevant articles and documents

Design and synthesis of depeptidized macrocyclic inhibitors of hepatitis C NS3-4A protease using structure-based drug design

Venkatraman, Srikanth,Njoroge, F. George,Girijavallabhan, Viyyoor M.,Madison, Vincent S.,Yao, Nanua H.,Prongay, Andrew J.,Butkiewicz, Nancy,Pichardo, John

, p. 5088 - 5091 (2007/10/03)

Hepatitus C virus (HCV) NS3, when bound to NS4A cofactor, facilitates development of mature virons by catalyzing cleavage of a polyprotein to form functional and structural proteins of HCV. The enzyme has a shallow binding pocket at the catalytic site, ma

Application of ruthenium induced cyclization for construction of strained biaryl ether macrocyclic compounds

Venkatraman, Srikanth,George Njoroge,Girijavallabhan, Viyyoor

, p. 5453 - 5458 (2007/10/03)

Synthesis of strained macrocyclic biaryl ethers of type 1 and 2 were accomplished using η6-ruthenium-induced macroetherification. This novel application demonstrates the versatility of this method in construction of constrained macrocyclic biar

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