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Benzoic acid, 5-[(3-chlorophenyl)azo]-2-[[(2,4-dichlorophenyl)methylene]amino]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

654649-10-2

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654649-10-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 654649-10-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,5,4,6,4 and 9 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 654649-10:
(8*6)+(7*5)+(6*4)+(5*6)+(4*4)+(3*9)+(2*1)+(1*0)=182
182 % 10 = 2
So 654649-10-2 is a valid CAS Registry Number.

654649-10-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-(m-chlorophenylazo)-N-(2,4-dichlorobenzylidene)anthranilic acid

1.2 Other means of identification

Product number -
Other names 5-(3-Chloro-phenylazo)-2-{[1-(2,4-dichloro-phenyl)-meth-(E)-ylidene]-amino}-benzoic acid

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:654649-10-2 SDS

654649-10-2Downstream Products

654649-10-2Relevant academic research and scientific papers

Synthesis of some newer derivatives of 2-amino benzoic acid as potent anti-inflammatory and analgesic agents

Kumar, Ashok,Bansal, Deepti,Bajaj, Kiran,Sharma, Shalabh,Archana,Srivastava

, p. 5281 - 5291 (2007/10/03)

Diazotization of N-benzylidene anthranilic acids 1a-1n at pH 9 yielded N-[α-(phenylazo) benzylidene] anthranilic acids 2a-2n and at pH 3 yielded N-benzylidene-5-(phenylazo) anthranilic acids 3a-3n. When compounds 3a-3n were treated with thioglycolic/thiolactic acid in the presence of anhydrous ZnCl 2, 2-(4-oxo-2-phenylthiazolidin-3-yl)-5-(phenylazo) benzoic acids 4a-4n were afforded. The newly synthesized compounds were screened for their anti-inflammatory and analgesic activities and were compared with standard drugs, aspirin and phenylbutazone. Out of the compounds studied, the most active compound 4n showed more potent activity than the standard drugs at all doses tested.

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