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1-<2-<(2-Methylphenyl)amino>phenyl>ethanon is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

23592-53-2

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23592-53-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 23592-53-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,5,9 and 2 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 23592-53:
(7*2)+(6*3)+(5*5)+(4*9)+(3*2)+(2*5)+(1*3)=112
112 % 10 = 2
So 23592-53-2 is a valid CAS Registry Number.

23592-53-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-[2-[(2-Methylphenyl)amino]phenyl]ethanon

1.2 Other means of identification

Product number -
Other names 2'-Methyl-2-acetyl-diphenylamin

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:23592-53-2 SDS

23592-53-2Relevant academic research and scientific papers

Selenium-promoted intramolecular oxidative amidation of 2-(arylamino)acetophenones for the synthesis of N-arylisatins

Liu, Yong,Chen, Hui,Hu, Xiong,Zhou, Wang,Deng, Guo-Jun

supporting information, p. 4229 - 4232 (2013/07/26)

A convenient method for the synthesis of N-arylisatins from 2-(arylamino)acetophenones by using SeO2 as an oxidant is described. Various substituted N-arylisatins were selectively obtained in good to excellent yields. The reaction tolerates a wide range of functionalities. Copyright

12-Organyldibenzazocine-5,7-diones

Hellwinkel, Dieter,Ittemann, Peter

, p. 3165 - 3197 (2007/10/02)

The title compounds 10, 23 are formed in low yields on treatment of 2,2'-organylimino-bisbenzoic acid esters 8 with methyllithium, but in high yields in the intramolecular ester condensation with sodium hydride of triarylamines 12, containing o-acetyl-, a

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