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Propanedioic acid, (2-phenyl-2-propenyl)-, also known as cinnamic acid, is an organic compound with the chemical formula C9H8O2. It is a colorless to white crystalline solid that is soluble in water, ethanol, and ether. Cinnamic acid is a derivative of propanoic acid, featuring a phenyl group attached to the propene side chain. Propanedioic acid, (2-phenyl-2-propenyl)- is widely used in the synthesis of various pharmaceuticals, fragrances, and flavorings due to its unique chemical properties and reactivity. It is also an important intermediate in the production of polymers and other organic compounds. Cinnamic acid is derived from the natural compound cinnamic aldehyde, which is found in the bark of cinnamon trees, and can also be synthesized through various chemical processes.

4469-65-2

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4469-65-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4469-65-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,4,6 and 9 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 4469-65:
(6*4)+(5*4)+(4*6)+(3*9)+(2*6)+(1*5)=112
112 % 10 = 2
So 4469-65-2 is a valid CAS Registry Number.

4469-65-2Relevant academic research and scientific papers

CYSTEINE PROTEASE INHIBITORS

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Page/Page column 49, (2010/02/07)

The present invention is directed to compounds that are inhibitors of cysteine protease, in particular, cathepsins B, K, L, F, and S and are therefore useful in treating diseases mediated by these proteases. The present invention is directed to pharmaceut

Research on cyclobutane compounds of biological interest. III. Syntheses and structure activity (antiinflammatory and antalgic) relationships of 3-substituted cyclobutane carboxylic acids

Escale,Girard,Vergnon,et al.

, p. 501 - 509 (2007/10/08)

Antiinflammatory and analgesic activities of 3 substituted cyclobutanecarboxylic acids are pointed out and their structure-activity relationship examined according to the Hansch method. This analysis shows the influence of the steric and lipophilic parameters and this quantitative basis let us realize the synthesis of two acids, the analgesic acitivities of which are very much improved. Attempted quantitative correlations between physiochemical parameters and antiinflammatory activity were unsuccessful. This is imputable to a too imprecise representation of the steric effect which plays a primordial part in this kind of activity.

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