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Ethyl 2-(4-fluorobenzyl)-3-oxo-3-phenylpropanoate is a complex organic compound with the molecular formula C19H17FO3. It is a derivative of propanoic acid, featuring a phenyl group at the third carbon and a 4-fluorobenzyl group at the second carbon. The molecule also contains an ester functional group, linking the carboxylic acid group to an ethyl group. ethyl 2-(4-fluorobenzyl)-3-oxo-3-phenylpropanoate is characterized by its aromatic structure and fluorine substitution, which can influence its reactivity and physical properties. It is typically synthesized for use in the pharmaceutical and chemical industries, where it may serve as an intermediate in the production of various drugs or other organic compounds. The specific applications and properties of ethyl 2-(4-fluorobenzyl)-3-oxo-3-phenylpropanoate can vary depending on the context in which it is used, but its unique structure makes it a potentially valuable component in the synthesis of specialized chemicals.

3830-53-3

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3830-53-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3830-53-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,8,3 and 0 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 3830-53:
(6*3)+(5*8)+(4*3)+(3*0)+(2*5)+(1*3)=83
83 % 10 = 3
So 3830-53-3 is a valid CAS Registry Number.

3830-53-3Downstream Products

3830-53-3Relevant academic research and scientific papers

Enantioselective and Diastereoselective Ir-Catalyzed Hydrogenation of α-Substituted β-Ketoesters via Dynamic Kinetic Resolution

Gu, Guoxian,Lu, Jiaxiang,Yu, Ouran,Wen, Jialin,Yin, Qin,Zhang, Xumu

, p. 1888 - 1892 (2018)

An iridium/f-amphol catalytic system for the enantioselective hydrogenation of α-substituted β-ketoesters via dynamic kinetic resolution is reported. The desired anti products were obtained in high yields (up to 98%) with good diastereoselectivity (up to 96:4 diastereometic ratio (dr)) and excellent enantioselectivity (up to >99% enantiomeric excess (ee)). A catalytic model is proposed to explain the stereoselectivity.

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