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Ethyl 2-fluoro-3-hydroxy-3-(4-methylphenyl)propanoate is a complex organic compound with the molecular formula C12H15FO3. It is a colorless liquid at room temperature and is soluble in most organic solvents. This chemical is characterized by the presence of a fluorine atom at the 2nd carbon, a hydroxyl group at the 3rd carbon, and a 4-methylphenyl group also attached to the 3rd carbon. The compound is an ester, formed by the reaction of the corresponding carboxylic acid with ethanol. It is used in the synthesis of various pharmaceuticals and agrochemicals due to its unique structure and reactivity. The compound's properties, such as its fluorine-containing structure, can impart specific biological activities, making it a valuable intermediate in the development of new drugs and pesticides.

1510-44-7

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1510-44-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1510-44-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,1 and 0 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1510-44:
(6*1)+(5*5)+(4*1)+(3*0)+(2*4)+(1*4)=47
47 % 10 = 7
So 1510-44-7 is a valid CAS Registry Number.

1510-44-7Downstream Products

1510-44-7Relevant academic research and scientific papers

Ethyl α-fluoro silyl enol ether: Stereoselective synthesis and its aldol reaction with aldehydes and ketones

Huang, Xiao-Ting,Chen, Qing-Yun

, p. 3231 - 3234 (2002)

Ethyl α-fluoro silyl enol ether is stereoselectively synthesized in high yield from inexpensive chlorofluoroacetate and Mg (or Zn) in DMF (or HMPA). Lewis acid promoted aldol reaction of this enol ether with aldehydes and ketones gives α-fluoro-β-hydroxy

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