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3-(5-chloro-2-methoxyphenyl)propanoic acid is a chemical compound with the molecular formula C10H11ClO3. It is an organic acid derived from propanoic acid, featuring a chlorinated and methoxylated phenyl group attached to the third carbon. 3-(5-chloro-2-methoxyphenyl)propanoic 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 provides a foundation for further chemical modifications, making it a valuable intermediate in the creation of more complex molecules. The presence of the chlorine atom and methoxy group on the phenyl ring can significantly influence the compound's reactivity and biological activity, which is why it is of interest in the fields of chemistry and drug design.

5553-96-8

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5553-96-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5553-96-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,5,5 and 3 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 5553-96:
(6*5)+(5*5)+(4*5)+(3*3)+(2*9)+(1*6)=108
108 % 10 = 8
So 5553-96-8 is a valid CAS Registry Number.

5553-96-8Relevant academic research and scientific papers

Small molecule inhibitors of anthrax lethal factor toxin

Williams, John D.,Khan, Atiyya R.,Cardinale, Steven C.,Butler, Michelle M.,Bowlin, Terry L.,Peet, Norton P.

, p. 419 - 434 (2014/01/17)

This manuscript describes the preparation of new small molecule inhibitors of Bacillus anthracis lethal factor. Our starting point was the symmetrical, bis-quinolinyl compound 1 (NSC 12155). Optimization of one half of this molecule led to new LF inhibitors that were desymmetrized to afford more drug-like compounds.

Phenalkoxyalkyl- and phenoxyalkyl-substituted oxiranecarboxylic acids, their use and medicaments containing them

-

, (2008/06/13)

Phenalkoxyalky- and phenoxyalkyl-substituted oxiranecarboxylic acids of the formula STR1 wherein R1 denotes a hydrogen atom (--H), a halogen atom, a lower alkyl group, a lower alkoxy group, a nitro group or a trifluoromethyl group, R2 has one of the meanings of R1, R3 denotes a hydrogen atom (--H) or a lower alkyl group, Y denotes --O--(CH2)m --, m denotes O or an integer from 1 to 4, and n denotes an integer from 2 to 8, with the proviso that the sum of m and n is an integer from 2 to 8, and the salts of the acids are new compounds. They display a hypoglycaemic action in warm-blooded animals. Processes for the preparation of the new compounds and of the intermediate products required for their preparation are described.

Substituted oxiranecarboxylic acids, their use and medicaments containing them

-

, (2008/06/13)

Substituted oxiranecarboxylic acids of the formula STR1 wherein R1 denotes a hydrogen atom (--H), a halogen atom, a hydroxylroup, a lower alkyl group, a lower alkoxy group or a trifluoromethyl group, R2 has one of the meanings of Rs

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