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2-(4-fluorobenzyl)aniline is an organic compound with the molecular formula C13H12FN. It is a derivative of aniline, featuring a 4-fluorobenzyl group attached to the 2-position of the aniline molecule. 2-(4-fluorobenzyl)aniline is characterized by its aromatic structure, with a fluorine atom in the para position of the benzyl group, which can influence its reactivity and physical properties. It is used in the synthesis of various pharmaceuticals and chemical intermediates, particularly in the development of compounds with potential applications in the fields of medicine and materials science. The presence of the fluorine atom can impart unique properties to the molecule, such as altered lipophilicity and metabolic stability, which are important considerations in drug design.

779-77-1

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779-77-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 779-77-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,7 and 9 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 779-77:
(5*7)+(4*7)+(3*9)+(2*7)+(1*7)=111
111 % 10 = 1
So 779-77-1 is a valid CAS Registry Number.

779-77-1Relevant academic research and scientific papers

Copper-Catalyzed One-Pot Synthesis of Dibenzofurans, Xanthenes, and Xanthones from Cyclic Diphenyl Iodoniums

Zhu, Daqian,Li, Min,Wu, Zhouming,Du, Yongliang,Luo, Bingling,Huang, Peng,Wen, Shijun

, p. 4566 - 4571 (2019/07/09)

Oxygenation of cyclic diphenyl iodoniums (CDPIs) with varied medium-ring sizes has been fully investigated. This practical copper-catalyzed tandem reaction of CDPIs with water as the oxygen source enables the construction of derivatised dibenzofurans and xanthenes at moderate to good yields. Moreover, structurally important xanthones are also successfully accessed under the oxygenation conditions with additional TEMPO.

Palladium-catalyzed decarboxylative coupling of potassium nitrophenyl acetates with aryl halides

Shang, Rui,Huang, Zheng,Chu, Ling,Fu, Yao,Liu, Lei

, p. 4240 - 4243 (2011/10/09)

A palladium-catalyzed decarboxylative cross-coupling of potassium 2- and 4-nitrophenyl acetates with aryl chlorides and bromides has been developed. Because the nitro group can be readily converted to many other functional groups, the new reaction provides a useful method for the preparation of diverse 1,1-diaryl methanes and their derivatives.

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