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3-bromo-2-phenylpropanoic acid is an organic compound with the chemical formula C9H9BrO2. It is a derivative of propanoic acid, featuring a bromine atom at the 3rd carbon position and a phenyl group attached to the 2nd carbon. This white crystalline solid is soluble in organic solvents and has a molecular weight of 229.07 g/mol. The compound is synthesized through various methods, such as the bromination of 2-phenylpropanoic acid or the carboxylation of 3-bromo-2-phenylpropene. It is used in the pharmaceutical industry as an intermediate for the synthesis of various drugs, including anti-inflammatory and analgesic medications. Due to its reactivity, it is essential to handle 3-bromo-2-phenylpropanoic acid with care, following proper safety protocols.

5441-68-9

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5441-68-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5441-68-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,4 and 1 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 5441-68:
(6*5)+(5*4)+(4*4)+(3*1)+(2*6)+(1*8)=89
89 % 10 = 9
So 5441-68-9 is a valid CAS Registry Number.

5441-68-9Relevant academic research and scientific papers

HYDROXAMATE SULFONAMIDES AS CD23 SHEDDING INHIBITORS

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Page 27, (2010/02/10)

A class of piperidine and related heterocyclic derivatives, C-substituted by a substituted aryl or heteroaryl moiety, and N-substituted by an ethylsulfonyl group which in turn is substituted at the 2-position by a hydroxamic acid moiety and also by a range of alternative substituents, being potent inhibitors of CD23 shedding, are useful in the treatment and/or prevention of allergic, inflammatory and neoplastic diseases.

HYDROXAMATE SULFONAMIDES AS CD23 SHEDDING INHIBITORS

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Page 30, (2010/02/10)

A class of piperazine and related heterocyclic derivatives, substituted at the 4-position by a substituted aryl or heteroaryl moiety, and at the 1-position by an ethylsulfonyl group which in turn is substituted at the 2-position by a hydroxamic acid moiety and also by a range of alternative substituents, being potent inhibitors of CD23 shedding, are useful in the treatment and/or prevention of allergic, inflammatory and neoplastic diseases.

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