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72236-23-8

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72236-23-8 Usage

General Description

3-(diethylcarbamoyl)benzoic acid is a chemical compound with the molecular formula C13H19NO3. It is a white crystalline solid that is soluble in organic solvents but insoluble in water. 3-(diethylcarbamoyl)benzoic acid is often used as a pharmaceutical intermediate in the synthesis of various drugs and as a corrosion inhibitor. It is also known for its ability to inhibit the enzyme COX-2, making it a potentially important compound in the development of anti-inflammatory drugs. Additionally, 3-(diethylcarbamoyl)benzoic acid has been studied for its potential use in the treatment of cancer due to its ability to inhibit cell growth and induce apoptosis in cancer cells. Overall, this chemical compound holds promise for various pharmaceutical and medical applications.

Check Digit Verification of cas no

The CAS Registry Mumber 72236-23-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,2,3 and 6 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 72236-23:
(7*7)+(6*2)+(5*2)+(4*3)+(3*6)+(2*2)+(1*3)=108
108 % 10 = 8
So 72236-23-8 is a valid CAS Registry Number.

72236-23-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(diethylcarbamoyl)benzoic acid

1.2 Other means of identification

Product number -
Other names 3-((Diethylamino)carbonyl)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:72236-23-8 SDS

72236-23-8Downstream Products

72236-23-8Relevant articles and documents

Microsomal metabolism of N,N-diethyl-m-toluamide (DEET, DET): The extended network of metabolites

Constantino, Luis,Iley, Jim

, p. 409 - 416 (1999)

The aim was to set out to establish the complete network of metabolites arising from the phenobarbital-treated rat liver microsomal oxidation of N,N-diethyl-m-toluamide (DEET). The products formed from DEET and all its subsequent metabolites were identifi

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