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4-carbamoyl-2,6-dimethylbenzoic acid is an organic compound with the molecular formula C10H11NO4. It is a derivative of benzoic acid, featuring a carbamoyl group (-CONH2) at the 4-position and two methyl groups (-CH3) at the 2 and 6 positions on the benzene ring. This chemical is known for its potential applications in the synthesis of pharmaceuticals and other organic compounds, particularly those with analgesic or anti-inflammatory properties. The compound's structure and functional groups contribute to its reactivity and ability to form various derivatives, making it a valuable intermediate in chemical synthesis.

7499-18-5

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7499-18-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7499-18-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,9 and 9 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 7499-18:
(6*7)+(5*4)+(4*9)+(3*9)+(2*1)+(1*8)=135
135 % 10 = 5
So 7499-18-5 is a valid CAS Registry Number.

7499-18-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-carbamoyl-2,6-dimethylbenzoic acid

1.2 Other means of identification

Product number -
Other names 4-Aminocarbonyl-2,6-dimethyl-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

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More Details:7499-18-5 SDS

7499-18-5Relevant academic research and scientific papers

ARYLOXY AND ARYLACYLOXY METHYL KETONES AS THIOL PROTEASE INHIBITORS

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, (2008/06/13)

Thiol protease inhibitors are disclosed having the formula: STR1 or an optical isomer thereof, or a pharmaceutically acceptable salt thereof, wherein:n is 0 or 1;m is 0, 1 or 2;X is H or an N-protecting group; each Y is independently an optionally protected α-amino acid residue;R is an optionally protected α-amino acid side chain that is H or CH 3 or that is bonded to the α-carbon atom to which it is attached by a methylene, methine or phenyl radical; andR' is optionally substituted aryl.

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