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Benzoic acid, 2-[(4-bromophenyl)amino]-4-chloro- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

90656-46-5

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90656-46-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 90656-46-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,6,5 and 6 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 90656-46:
(7*9)+(6*0)+(5*6)+(4*5)+(3*6)+(2*4)+(1*6)=145
145 % 10 = 5
So 90656-46-5 is a valid CAS Registry Number.

90656-46-5SDS

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 2-(4-bromoanilino)-4-chlorobenzoic acid

1.2 Other means of identification

Product number -
Other names Benzoic acid,2-[(4-bromophenyl)amino]-4-chloro

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:90656-46-5 SDS

90656-46-5Relevant academic research and scientific papers

PhI(OAc)2-mediated intramolecular oxidative aryl-aldehyde C sp 2-C sp 2 bond formation: Metal-free synthesis of acridone derivatives

Zheng, Zisheng,Dian, Longyang,Yuan, Yucheng,Zhang-Negrerie, Daisy,Du, Yunfei,Zhao, Kang

, p. 7451 - 7458 (2014/09/17)

A metal-free protocol for direct aryl-aldehyde Csp2-Csp 2 bond formation via a PhI(OAc)2-mediated intramolecular cross-dehydrogenative coupling (CDC) of various 2-(N-arylamino)aldehydes was developed. The novel methodology requires no need of preactivation of the aldehyde group, is applicable to a large variety of functionalized substrates, and most of all provides a convenient approach to the construction of biologically important acridone derivatives.

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