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2-bromo-4-(methylsulfonyl)benzoic acid is an organic compound characterized by its molecular formula C8H7BrO4S. 2-bromo-4-(methylsulfonyl)benzoic acid features a benzoic acid backbone with a bromine atom at the 2-position and a methylsulfonyl group attached at the 4-position. The presence of the bromine atom and the methylsulfonyl group imparts unique chemical properties to the molecule, making it a potentially valuable intermediate in the synthesis of various pharmaceuticals and agrochemicals. Its structure and reactivity can be exploited in organic synthesis, particularly in reactions involving electrophilic aromatic substitution and nucleophilic substitution, due to the activating effect of the methylsulfonyl group on the benzene ring.

7041-52-3

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7041-52-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7041-52-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,0,4 and 1 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 7041-52:
(6*7)+(5*0)+(4*4)+(3*1)+(2*5)+(1*2)=73
73 % 10 = 3
So 7041-52-3 is a valid CAS Registry Number.

7041-52-3Relevant academic research and scientific papers

2,3-DIHYDROQUINAZOLIN COMPOUNDS AS NAV1.8 INHIBITORS

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Page/Page column 161; 169, (2021/01/23)

The present invention relates to Nav1.8 Inhibitor 2,3-dihydroquinazolin compounds of Formula (X); wherein Y', X', B', R1', R2', R3', R5', R6', R7', and z1 are as defined herein; or pharmaceutically acceptable salts or tautomer forms thereof, corresponding pharmaceutical compositions or formulations, methods or processes of compound preparation, methods, compounds for use in, uses for and/or combination therapies for treating pain and/or pain-related or associated disease(s), disorder(s) or condition(s), respectively.

Preparation of 2-(chloro, bromo or nitro)-4-(alkyl-sulfonyl)benzoic acids and intermediates

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, (2008/06/13)

A process for the preparation of 2-(chloro, bromo or nitro)-4-(alkylsulfonyl)benzoic acid and to intermediates used in the process.

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