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2,4-difluoro-α-methyldihydrocinnamic acid is a chemical compound with the molecular formula C11H11F2O2, derived from cinnamic acid, a common organic compound found in various plants. This specific compound is distinguished by the presence of two fluorine atoms and a methyl group on the cinnamic acid structure, which endows it with unique properties and potential applications in organic synthesis and pharmaceutical research.

32004-71-0

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32004-71-0 Usage

Uses

Used in Organic Synthesis:
2,4-difluoro-α-methyldihydrocinnamic acid is used as a building block in organic synthesis for its potential to serve as a precursor for various bioactive compounds. The presence of fluorine and methyl groups on the cinnamic acid structure allows for the creation of a diverse range of chemical entities with different biological activities.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 2,4-difluoro-α-methyldihydrocinnamic acid is used as a starting material for the development of new drugs. Its unique combination of fluorine and methyl substituents makes it of interest for medicinal chemistry and drug discovery applications, as these modifications can influence the pharmacokinetics, potency, and selectivity of the resulting compounds.
Used in Medicinal Chemistry:
2,4-difluoro-α-methyldihydrocinnamic acid is utilized in medicinal chemistry for the design and synthesis of novel therapeutic agents. The incorporation of fluorine atoms can enhance the lipophilicity, metabolic stability, and receptor binding affinity of the resulting compounds, while the methyl group can modulate the steric and electronic properties of the molecule, leading to improved drug candidates.
Used in Drug Discovery:
In drug discovery, 2,4-difluoro-α-methyldihydrocinnamic acid is employed as a versatile template for the exploration of new chemical space and the identification of potential lead compounds. Its structural features make it a valuable tool for the optimization of drug-like properties and the generation of novel bioactive molecules with therapeutic potential.

Check Digit Verification of cas no

The CAS Registry Mumber 32004-71-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,2,0,0 and 4 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 32004-71:
(7*3)+(6*2)+(5*0)+(4*0)+(3*4)+(2*7)+(1*1)=60
60 % 10 = 0
So 32004-71-0 is a valid CAS Registry Number.

32004-71-0Upstream product

32004-71-0Relevant academic research and scientific papers

Method for treating patient having precancerous lesions with a combination of pyrimidopyrimidine derivatives and esters and amides of substituted indenyl acetic acides

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, (2008/06/13)

Combinations of substituted indenyl acetic acids and pyrimido-pyrimidine derivatives are useful in the treatment of colonic polyps and inhibiting the growth of neoplastic cells.

Substituted methoxy benzylidene indenyl-acetic and propionic acids for treating patients with precancerous lesions

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, (2008/06/13)

Substituted methoxy benzylidene indenyl compounds are useful in the treatment of precancerous lesions and neoplasms.

Method for treating patients with precancerous lesions by administering substituted sulfonyl idenyl acetic and propionic acids and esters to patients with lesions sensitive to such compounds

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, (2008/06/13)

Substituted indenyl sulfonyl acetic acids are useful in the treatment of precancerous lesions sensitive to treatment with those sulfonyl compounds.

Esters and amides of substituted indenyl acetic acids

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, (2008/06/13)

Esters and amides of substituted indenyl acetic acids of the formula: n is an integer of at least 2;, Q is a deprotonated residue of polymer or macromolecular structure having a molecular weight of at least about 1000 containing at least two primary and/or secondary amino groups and/or hydroxy groups;, R1 is selected from hydrogen, lower alkyl, or haloalkyl;, R2 is selected from hydrogen or alkyl;, R3 and R4 are one or more members each independently chosen from hydrogen, alkyl, acyloxy, alkoxy, nitro, amino, acylamino, alkylamino, diakylamino, dialkylaminoalkyl, sulfamyl, alkythio, mercapto, hydroxy, hydroxyalkyl, alkylsulfonyl, halogen, cyano, carboxyl, carbalkoxy, carbamido, haloalkyl or cycloalkoxy; and, R5 is selected from alkylsulfenyl, alkylsulfinyl or alkylsulfonyl. are useful in the treatment of colonic polyps.

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