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174878-38-7

174878-38-7

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174878-38-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 174878-38-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,4,8,7 and 8 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 174878-38:
(8*1)+(7*7)+(6*4)+(5*8)+(4*7)+(3*8)+(2*3)+(1*8)=187
187 % 10 = 7
So 174878-38-7 is a valid CAS Registry Number.

174878-38-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-bromo-N-(6-methylpyridin-2-yl)benzamide

1.2 Other means of identification

Product number -
Other names BENZAMIDE,4-BROMO-N-(6-METHYL-2-PYRIDINYL)-

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:174878-38-7 SDS

174878-38-7Downstream Products

174878-38-7Relevant articles and documents

Synthesis of a dicarboxylic acid receptor organized around a dioxomolybdenum core

Prevot-Halter, Isabelle,Smith, Thomas J.,Weiss, Jean

, p. 1201 - 1204 (1996)

-

A one-pot copper catalyzed biomimetic route to n -heterocyclic amides from methyl ketones via oxidative c-c bond cleavage

Subramanian, Parthasarathi,Indu, Satrajit,Kaliappan, Krishna P.

supporting information, p. 6212 - 6215 (2015/01/09)

A direct one-pot Cu-catalyzed biomimetic oxidation of methyl ketones to pharmaceutically important N-heterocyclic amides is reported. The scope of the method is broad, scalable, and mild, and the reaction is tolerant with various acid, base sensitive functionalities with multiple heteroatoms and aryl halides. The extensive mechanistic studies suggest that this reaction follows the Luciferin-Luciferase-like pathway.

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