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Benzenecarboximidamide, N-(1,2-diphenylethenyl)-, (E)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

76005-90-8

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76005-90-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 76005-90-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,0,0 and 5 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 76005-90:
(7*7)+(6*6)+(5*0)+(4*0)+(3*5)+(2*9)+(1*0)=118
118 % 10 = 8
So 76005-90-8 is a valid CAS Registry Number.

76005-90-8SDS

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 N-(diphenyl-1,2) vinylbenzamidine

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:76005-90-8 SDS

76005-90-8Relevant academic research and scientific papers

PYRIDINES, PARTIE X - SYNTHESE DE PYRIDYL- ET QUINOLYLENAMIDINES PAR CONDENSATION ENTRE COMPOSES ORGANOLITHIENS ET BENZONITRILE. NOVEAUX INTERMEDIAIRES POUR REACTIONS D'HETEROCYCLISATION

Compagnon, Paul-Luis,Gasquez, Francoise,Compagnon, Odette,Kimny, Tan

, p. 931 - 946 (2007/10/02)

A series of methylpyridyl- and (methyl)quinolylphenylvinylbenzamidines has been synthesized by condensation of organopolylithium compounds derived from polymethylpyridines and quinolines with benzonitrile.In diethyl ether, besides the enamidines, the reaction gives enolizable ketones.Triphenylimidazole, triphenyl-s-triazine and triphenylpyrimidine are isolated in the case of benzylmagnesium chloride.Possible routes leading to the various products are suggested.In diethyl ether, the conditions wich give the enamidine derivatives in useful yields have been established.In liquid ammonia, on the contrary, no polycondensed products were isolated.The intermediate enamine and enamidine anions are trapped in diethyl ether by acetylation of the reaction mixture before hydrolysis.With benzoyl or acetyl chloride, ethyl chloroformate, various C- and N-acylated products (enolizable β-diketones, enamides, acylenamides, N-acylenamidines) and their cyclization products (pyrimidines) are obtained.The latter are also prepared from the isolated enamidines and benzoyl chlorides.

Enamidines. Part 1. Synthesis of Enamidines and Dihydrotriazines by the Reaction of Organolithium and Organomagnesium Compounds with Aromatic Nitriles

Cook, Lawrence S.,Wakefield, Basil J.

, p. 2392 - 2397 (2007/10/02)

The reaction of alkyl-lithium compounds, possessing α-hydrogens, or benzylmagnesium chloride with aromatic nitriles, followed by hydrolysis, gives ketones, E- and Z-N1-(arylalk-1-enyl)benzamidines, 2-alkyl-2,4,6-triaryldihydro-1,3,5-triazines, and 2,4,6-triaryl-1,3,5-triazines.Conditions for preparing the enamidines in useful yields were established. t-Butyl-lithium and phenyl-lithium with benzonitrile gave only the ketones and dihydrotriazines.Phenylmagnesium bromide gave only benzophenone.

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