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1H-Imidazole, 4-methyl-1-(3-methyl-4-nitrophenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

102791-94-6

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102791-94-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 102791-94-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,2,7,9 and 1 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 102791-94:
(8*1)+(7*0)+(6*2)+(5*7)+(4*9)+(3*1)+(2*9)+(1*4)=116
116 % 10 = 6
So 102791-94-6 is a valid CAS Registry Number.

102791-94-6SDS

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 5-(4-methylimidazol-1-yl)-2-nitrotoluene

1.2 Other means of identification

Product number -
Other names 4-Methyl-1-(3-methyl-4-nitro-phenyl)-1H-imidazole

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:102791-94-6 SDS

102791-94-6Relevant academic research and scientific papers

Imidazole substituted benzoxazine or benzothiazine derivatives

-

, (2008/06/13)

A benzoxazine or benzothiazine derivative of the formula (A), STR1 wherein R1, R2 and R3 are the same or different and represent a hydrogen atom or a C1-4 alkyl group; or R1 and R2 can be j

Novel benzoxazine or benzothiazine derivatives and process for the preparation of the same

-

, (2008/06/13)

Novel benzoxazine or benzothiazine derivatives of the formaula(A), wherein R1, R2 and R3 are the same or different and represent hydrogen atom or C1 4 lower alkyl group and X and Y are the same or dif

2(1H)-Quinolinones with cardiac stimulant activity. 2. Synthesis and biological activities of 6-(N-linked, five membered heteroaryl) derivatives

Alabaster,Bell,Campbell,Ellis,Henderson,Morris,Roberts,Ruddock,Samuels,Stefaniak

, p. 575 - 583 (2007/10/02)

A series of 6-(N-linked, five membered heteroaryl)-2(1H)-quinolinone derivatives was synthesized and evaluated for cardiotonic activity. Most compounds were prepared by sulfuric acid catalyzed cyclization of an N-(4-heteroarylphenyl)-3-ethoxypropenamide o

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