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Benzoicacid, 2-[(2,4-dichlorophenyl)methylene]hydrazide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

39575-07-0

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39575-07-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 39575-07-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,5,7 and 5 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 39575-07:
(7*3)+(6*9)+(5*5)+(4*7)+(3*5)+(2*0)+(1*7)=150
150 % 10 = 0
So 39575-07-0 is a valid CAS Registry Number.

39575-07-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name N-[(2,4-dichlorophenyl)methylideneamino]benzamide

1.2 Other means of identification

Product number -
Other names 1,3,5-Benzenetricarbonitrile,2-(bromoanilino)-4,6-dichloro

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:39575-07-0 SDS

39575-07-0Relevant academic research and scientific papers

I2-mediated oxidative C-O bond formation for the synthesis of 1,3,4-oxadiazoles from aldehydes and hydrazides

Yu, Wenquan,Huang, Gang,Zhang, Yueteng,Liu, Hongxu,Dong, Lihong,Yu, Xuejun,Li, Yujiang,Chang, Junbiao

, p. 10337 - 10343 (2013/11/06)

A practical and transition-metal-free oxidative cyclization of acylhydrazones into 1,3,4-oxadiazoles has been developed by employing stoichiometric molecular iodine in the presence of potassium carbonate. The conditions of this cyclization reaction also work well with crude acylhydrazone substrates obtained from the condensation of aldehydes and hydrazides. A series of symmetrical and asymmetrical 2,5-disubstituted (aryl, alkyl, and/or vinyl) 1,3,4-oxadiazoles can be conveniently generated in an efficient and scalable fashion.

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