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(4-fluorophenyl)dimethyl(vinyl)silane is an organosilicon compound characterized by a vinyl group attached to a silicon atom, which is further bonded to a 4-fluorophenyl group and two methyl groups. This chemical structure endows the compound with unique properties, such as reactivity and stability, making it useful in various applications, including the synthesis of polymers, pharmaceuticals, and materials science. The presence of the fluorine atom in the phenyl ring can influence the electronic properties and reactivity of the molecule, while the vinyl group provides a point of unsaturation that can participate in addition reactions, making (4-fluorophenyl)dimethyl(vinyl)silane a versatile building block in organic synthesis.

29886-51-9

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29886-51-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 29886-51-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,8,8 and 6 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 29886-51:
(7*2)+(6*9)+(5*8)+(4*8)+(3*6)+(2*5)+(1*1)=169
169 % 10 = 9
So 29886-51-9 is a valid CAS Registry Number.

29886-51-9Downstream Products

29886-51-9Relevant academic research and scientific papers

Cross-Electrophile C(sp2)?Si Coupling of Vinyl Chlorosilanes

Duan, Jicheng,Kang, Shaolin,Liu, Xue-Yuan,Qi, Liangliang,Shu, Xing-Zhong,Wang, Ke,Xu, Guang-Li

supporting information, p. 23083 - 23088 (2020/12/09)

The cross-electrophile coupling has become a powerful tool for C?C bond formation, but its potential for forging the C?Si bond remains unexplored. Here we report a cross-electrophile Csp2-Si coupling reaction of vinyl/aryl electrophiles with vinyl chlorosilanes. This new protocol offers an approach for facile and precise synthesis of organosilanes with high molecular diversity and complexity from readily available materials. The reaction proceeds under mild and non-basic conditions, demonstrating a high step economy, broad substrate scope, wide functionality tolerance, and easy scalability. The synthetic utility of the method is shown by its efficient accessing of silicon bioisosteres, the design of new BCB-monomers, and studies on the Hiyama cross-coupling of vinylsilane products.

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