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Pyridinium, 3-(aminocarbonyl)-2-methyl-1-(phenylmethyl)-, bromide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

114174-71-9

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114174-71-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 114174-71-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,4,1,7 and 4 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 114174-71:
(8*1)+(7*1)+(6*4)+(5*1)+(4*7)+(3*4)+(2*7)+(1*1)=99
99 % 10 = 9
So 114174-71-9 is a valid CAS Registry Number.

114174-71-9SDS

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 1-benzyl-2-methyl-3-carbamoylpyridinium bromide

1.2 Other means of identification

Product number -
Other names N-benzyl-2-methylnicotinamidinium bromide

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:114174-71-9 SDS

114174-71-9Relevant academic research and scientific papers

Thermodynamic characteristics of NADH/NAD+ analogues in acetonitrile: 2-methyl, 4-methyl and 2,4-dimethyl 1-benzyl-dihydronicotinamides and the corresponding pyridinium species

Anne,Moiroux

, p. 531 - 538 (2007/10/02)

Procedures were elaborated for the syntheses of the title compounds. The thermodynamic changes brought about by each methyl substitution were then determined quantitatively. In acetonitrile, the respective one-electron oxidation and one-electron reduction

Steric and Electronic Effects of Methyl Substitutents at the 2- and 6-Positions on N-Benzyl-1,4-dihydronicotinamide

Takeda, Jun,Ohta, Shigeru,Hirobe, Masaaki

, p. 2661 - 2667 (2007/10/02)

N-Benzyl-1,4-dihydronicotinamides having 2-methyl, 6-methyl and 2,6-dimethyl substituents were prepared and their reactivities toward an activated carbonyl compound (hexachloroacetone) were investigated.The reaction rates were especially enhanced for the

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