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111566-79-1

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111566-79-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 111566-79-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,1,5,6 and 6 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 111566-79:
(8*1)+(7*1)+(6*1)+(5*5)+(4*6)+(3*6)+(2*7)+(1*9)=111
111 % 10 = 1
So 111566-79-1 is a valid CAS Registry Number.

111566-79-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-iodo-2-methyl-1-(3-methyl-4-nitrophenyl)imidazole

1.2 Other means of identification

Product number -
Other names 1-(3-Methyl-4-nitrophenyl)-4-iodo-2-methylimidazole

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:111566-79-1 SDS

111566-79-1Relevant articles and documents

2(1H)-Quinolinones with Cardiac Stimulant Activity. 3. Synthesis and Biological Properties of 6-Imidazol-1-yl Derivatives

Bell, Andrew S.,Campbell, Simon F.,Morris, David S.,Roberts, David A.,Stefaniak, Mark H.

, p. 1552 - 1558 (2007/10/02)

A series of 6-imidazol-1-yl-8-methyl-2(1H)-quinolinones was synthesized and evaluated for cardiac stimulant activity in dogs.The majority of compounds were prepared from an appropriate 6-imidazol-1-yl-2(1H)-quinolinone precursor or by sulfuric acid cataly

Methyl substituted imidazol-1-yl quinolones

-

, (2008/06/13)

A series of novel heterocyclic-substituted 2-(1H)-quinolone compounds have been prepared wherein the heterocyclic ring moiety is a substituted pyrrolyl, imidazolyl, pyrazolyl, triazolyl or tetrazolyl group attached by a nitrogen atom of said group to the

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