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(2-fluoro-ethyl)-(4-fluoro-phenyl)-ether is an organic compound characterized by its molecular structure, which consists of a fluoro-phenyl group attached to an ether linkage, with a fluoro-ethyl group on the opposite side. (2-fluoro-ethyl)-(4-fluoro-phenyl)-ether is a derivative of diphenyl ether, with fluorine atoms substituting hydrogen atoms at the 2nd position of the ethyl group and the 4th position of the phenyl group. The presence of fluorine atoms imparts unique properties to the molecule, such as increased lipophilicity and potential reactivity differences compared to non-fluorinated analogs. (2-fluoro-ethyl)-(4-fluoro-phenyl)-ether may be of interest in various chemical and pharmaceutical applications due to its specific structural features and the influence of fluorine on its physical and chemical properties.

659-36-9

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659-36-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 659-36-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,5 and 9 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 659-36:
(5*6)+(4*5)+(3*9)+(2*3)+(1*6)=89
89 % 10 = 9
So 659-36-9 is a valid CAS Registry Number.

659-36-9Downstream Products

659-36-9Relevant academic research and scientific papers

Direct Deoxyfluorination of Alcohols with KF as the Fluorine Source

Xu, Jun,Peng, Chao,Yao, Bolin,Xu, Hua-Jian,Xie, Qiang

, p. 6471 - 6478 (2022/05/07)

This report describes a method for the deoxyfluorination of alcohols with KF as the fluorine source via in situ generation of highly active CF3SO2F. Diverse functionalities, including halogen, nitro, ketone, ester, alkene, and alkyne, are well tolerated. Mild conditions, a short reaction time, and a wide substrate scope make this method an excellent choice for the construction of C-F bonds.

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