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(E)-2-(4-Chloro-phenyl)-3-fluoro-prop-2-en-1-ol is a chemical compound characterized by its molecular structure, which features a 3-fluoroprop-2-en-1-ol group attached to a 4-chlorophenyl ring. This molecule is an enol, indicating the presence of a hydroxyl group (-OH) bonded to a carbon atom that is also part of a carbon-carbon double bond. The "E" configuration refers to the geometric isomerism around the double bond, where the fluorine and chlorine substituents are on opposite sides of the double bond. (E)-2-(4-Chloro-phenyl)-3-fluoro-prop-2-en-1-ol is a derivative of phenol, with a fluorinated and chlorinated alkene side chain, which may have applications in the synthesis of pharmaceuticals or other organic compounds due to its unique electronic and steric properties.

85277-91-4

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85277-91-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 85277-91-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,2,7 and 7 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 85277-91:
(7*8)+(6*5)+(5*2)+(4*7)+(3*7)+(2*9)+(1*1)=164
164 % 10 = 4
So 85277-91-4 is a valid CAS Registry Number.

85277-91-4Relevant academic research and scientific papers

Enzyme-activated irreversible inhibitors of monoamine oxidase: Phenylallylamine structure-activity relationships

McDonald,Lacoste,Bey,Palfreyman,Zreika

, p. 186 - 193 (2007/10/02)

Seventeen 2-aryl-3-haloallylamine derivatives were prepared and evaluated as inhibitors of monoamine oxidase (MAO, EC 1.4.3.4). The synthesis of these compounds was achieved from either α-methylstyrene or ring-substituted phenylacetic acid derivatives. Wi

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