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4-Methanesulfonylamino-2-methylbenzoic acid is a chemical compound with the molecular formula C10H11NO4S. It is a derivative of benzoic acid, featuring a methanesulfonyl group (-SO2CH3) attached to the 4-position and a methyl group (-CH3) at the 2-position. 4-methanesulfonylamino-2-methylbenzoic acid is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals, particularly as a building block for the development of new drugs. Its structure allows for further chemical modifications, making it a versatile intermediate in organic synthesis. The compound is typically synthesized through a series of reactions involving benzoic acid and other reagents, and it is characterized by its ability to form salts and esters, which can be used in different chemical processes.

960324-76-9

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960324-76-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 960324-76-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,6,0,3,2 and 4 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 960324-76:
(8*9)+(7*6)+(6*0)+(5*3)+(4*2)+(3*4)+(2*7)+(1*6)=169
169 % 10 = 9
So 960324-76-9 is a valid CAS Registry Number.

960324-76-9Downstream Products

960324-76-9Relevant academic research and scientific papers

Solid-phase parallel synthesis and SAR of 4-amidofuran-3-one inhibitors of cathepsin S: Effect of sulfonamides P3 substituents on potency and selectivity

Ayesa, Susana,Lindquist, Charlotta,Agback, Tatiana,Benkestock, Kurt,Classon, Bjoern,Henderson, Ian,Hewitt, Ellen,Jansson, Katarina,Kallin, Anders,Sheppard, Dave,Samuelsson, Bertil

experimental part, p. 1307 - 1324 (2009/08/08)

Highly potent and selective 4-amidofuran-3-one inhibitors of cathepsin S are described. The synthesis and structure-activity relationship of a series of inhibitors with a sulfonamide moiety in the P3 position is presented. Several members of the series show sub-nanomolar inhibition of the target enzyme as well as an excellent selectivity profile and good cellular potency. Molecular modeling of the most interesting inhibitors describes interactions in the extended S3 pocket and explains the observed selectivity towards cathepsin K.

BICYCLIC COMPOUNDS USEFUL AS CATHEPSIN S INBHIBITORS

-

, (2010/11/29)

Compounds of formula (I), wherein R1, R2, R3, Ra and E are are defined within, and pharmaceutically acceptable salts, solvates, hydrates and N-oxides thereof having utility in the treatment of disorders mediated by cathepsin S.

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