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Benzenamine, 3-methyl-N-(1-phenylethylidene)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

26625-24-1

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26625-24-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 26625-24-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,6,2 and 5 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 26625-24:
(7*2)+(6*6)+(5*6)+(4*2)+(3*5)+(2*2)+(1*4)=111
111 % 10 = 1
So 26625-24-1 is a valid CAS Registry Number.

26625-24-1SDS

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-(3-methylphenyl)-1-phenylethanimine

1.2 Other means of identification

Product number -
Other names N-(1-Phenyl-aethyliden)-m-toluidin

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:26625-24-1 SDS

26625-24-1Relevant academic research and scientific papers

From Ketones, Amines, and Carbon Monoxide to 4-Quinolones: Palladium-Catalyzed Oxidative Carbonylation

Wu, Jiwei,Zhou, Yuchen,Wu, Ting,Zhou, Yi,Chiang, Chien-Wei,Lei, Aiwen

supporting information, p. 6432 - 6435 (2017/12/08)

A novel method of palladium-catalyzed oxidative carbonylation of ketones, amines, and carbon monoxide for the synthesis of 4-quinolones has been developed. This protocol provides a straightforward route to construct useful 4-quinolone derivatives from ine

Zirconium complexes stabilized by amine-bridged bis(phenolato) ligands as precatalysts for intermolecular hydroamination reactions

Sun, Qiu,Wang, Yaorong,Yuan, Dan,Yao, Yingming,Shen, Qi

, p. 20352 - 20360 (2015/12/04)

A series of zirconium complexes bearing amine-bridged bis(phenolato) ligands of different steric and electronic properties have been synthesized, and their activities in catalyzing intermolecular hydroamination reactions have been studied and compared. In

Synthesis of group 4 metal complexes stabilized by an amine-bridged bis(phenolato) ligand and their catalytic behavior in intermolecular hydroamination reactions

Sun, Qiu,Wang, Yaorong,Yuan, Dan,Yao, Yingming,Shen, Qi

, p. 994 - 1001 (2014/03/21)

Zirconium and titanium complexes 1 and 2, bearing an amine-bridged bis(phenolato) ligand, have been synthesized and characterized. Although 1 and 2 were inactive in catalyzing intermolecular hydroamination reactions, cationic complexes generated in situ f

The potassium hydride mediated trimerization of imines

Kutlescha, Kathrin,Venkanna, Gopaladasu T.,Kempe, Rhett

supporting information; experimental part, p. 4183 - 4185 (2011/06/25)

A novel reaction, the potassium hydride mediated synthesis of fulvenes, is described. The synthesis utilizes N-aryl imines as an inexpensive starting material affording novel substituted aminofulvenes. It is proposed that the presence of the metalated enamine as well as the imine (ratio 21) leads to the formation of an initial dimerization and a transient trimerization product, which cyclizes, giving rise to the aminofulvene.

Novel amido-complexes for the efficient asymmetric hydrogenation of imines

Kutlescha, Kathrin,Irrgang, Torsten,Kempe, Rhett

supporting information; experimental part, p. 3126 - 3130 (2011/02/22)

Novel N,N,P ligand stabilized rhodium complexes exhibiting high activities and enantioselectivities in the asymmetric hydrogenation of N-aryl imines are introduced. The ligands were synthesized from inexpensive starting materials and their modular design

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