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(1-fluoroethene-1,2-diyl)dibenzene, also known as 1,2-difluoro-1,2-bis(phenyl)ethene or 1,2-diphenylethene-1,2-difluoride, is an organic compound with the molecular formula C14H10F2. It is a colorless liquid that is insoluble in water but soluble in organic solvents. (1-fluoroethene-1,2-diyl)dibenzene is characterized by the presence of a fluoroethene (fluorinated ethylene) group bridging two benzene rings, which imparts unique chemical and physical properties. It is synthesized through various methods, including the reaction of benzene with fluoroacetic acid derivatives. (1-fluoroethene-1,2-diyl)dibenzene has potential applications in the fields of material science and pharmaceuticals, particularly as a building block for the synthesis of more complex fluorinated organic compounds. Due to its fluorine content, it may exhibit different reactivity and stability compared to its non-fluorinated analogs, making it a subject of interest in chemical research.

717-13-5

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717-13-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 717-13-5 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,1 and 7 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 717-13:
(5*7)+(4*1)+(3*7)+(2*1)+(1*3)=65
65 % 10 = 5
So 717-13-5 is a valid CAS Registry Number.

717-13-5Relevant academic research and scientific papers

Gold-Catalyzed Hydrofluorination of Internal Alkynes Using Aqueous HF

Gauthier, Rapha?l,Mamone, Marius,Paquin, Jean-Fran?ois

supporting information, p. 9024 - 9027 (2019/11/14)

The gold-catalyzed hydrofluorination reaction of internal alkynes using hydrofluoric acid is reported. Notably, those conditions use one of the most economical sources of HF and are free of additional additives. Both symmetrical and unsymmetrical internal alkynes can be utilized, and the use of alkynes bearing a fluorinated group at the propargylic position as substrates allowed for a regioselective hydrofluorination reaction.

Facile preparation of fluorine-containing alkenes, amides and alcohols via the electrophilic fluorination of alkenyl boronic acids and trifluoroborates

Petasis, Nicos A.,Yudin, Andrei K.,Zavialov, Ilia A.,Prakash, G. K. Surya,Olah, George A.

, p. 606 - 608 (2007/10/03)

Reaction of alkenyl boronic acids, or preferably alkenyl trifluoroborates, with one equivalent of Selectfluor gives the corresponding alkenyl fluorides. A similar reaction with two equivalents of Selectfluor in water or a nitrile solvent gives difluoromet

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