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Benzoic acid, 4-methyl-, 1-methylhydrazide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

79129-59-2

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79129-59-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 79129-59-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,1,2 and 9 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 79129-59:
(7*7)+(6*9)+(5*1)+(4*2)+(3*9)+(2*5)+(1*9)=162
162 % 10 = 2
So 79129-59-2 is a valid CAS Registry Number.

79129-59-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name N,4-dimethylbenzohydrazide

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:79129-59-2 SDS

79129-59-2Relevant academic research and scientific papers

Synthesis of phthalazinones via palladium(ii)-catalysed intramolecular oxidative C-H/C-H cross-coupling of N′-methylenebenzohydrazides

Matsuda, Takanori,Tomaru, Yuki,Matsuda, Yoshiya

supporting information, p. 2084 - 2087 (2013/04/23)

A palladium(ii)-catalysed intramolecular oxidative C-H/C-H cross-coupling of N′-methylenebenzohydrazides to phthalazin-1(2H)-ones has been developed. This cyclization is believed to mechanistically proceed via electrophilic ortho-palladation and subsequen

An efficient synthesis of substituted hydrazides

Benstead, David J.,Hulme, Alison N.,McNab, Hamish,Wight, Paul

, p. 1571 - 1574 (2007/10/03)

Routes for the selective synthesis of 1-, or 2-substituted hydrazides, and 1,2-disubstituted hydrazides are reported. These routes proceed via cyanoborohydride reduction of stable acyl hydrazone intermediates. Georg Thieme Verlag Stuttgart.

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