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5-methyl-2-(propan-2-yl)phenyl 2-[(2,3-dimethylphenyl)amino]benzoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

20724-12-3

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20724-12-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 20724-12-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,7,2 and 4 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 20724-12:
(7*2)+(6*0)+(5*7)+(4*2)+(3*4)+(2*1)+(1*2)=73
73 % 10 = 3
So 20724-12-3 is a valid CAS Registry Number.

20724-12-3SDS

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-methyl-2-propan-2-ylphenyl) 2-(2,3-dimethylanilino)benzoate

1.2 Other means of identification

Product number -
Other names Anthranilic acid,N-2,3-xylyl-,thymyl ester

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:20724-12-3 SDS

20724-12-3Downstream Products

20724-12-3Relevant academic research and scientific papers

Evaluation of mefenamic acid mutual prodrugs

Shah, Kamal,Shrivastava, Sushant K.,Mishra, Pradeep

, p. 70 - 77 (2013)

Mutual prodrugs consisting of mefenamic acid with menthol and thymol have been synthesized as a gastrosparing NSAIDs, devoid of ulcerogenic side effects. The structures of synthesized esters were confirmed by IR, 1H NMR, and mass spectroscopy. The kinetics of ester hydrolysis was studied in nonenzymatic buffer solutions, at pH 2 and 7.4 as well as in human plasma by HPLC. Its anti-inflammatory, analgesic, and ulcerogenic activities were evaluated. Then biochemical parameters (GWM and Hexosamine), oxidative parameters (LPO, GSH, CAT, and SOD), and protein estimation was also done. The results indicated that synthesized prodrugs are chemically stable, biolabile, and posses optimum lipophilicity. The synthesized prodrugs are characterized by better ulcer index than the parent drug.

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