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Cyclohex-2-enyldiphenylsilane is an organosilicon compound with the chemical formula C18H20Si. It features a cyclohexene ring with a double bond at the 2-position, which is connected to two phenyl groups (C6H5) and a silyl group (SiH3). cyclohex-2-enyldiphenylsilane is known for its unique structure, which combines the properties of both organic and inorganic components. It is used in various chemical reactions, particularly in the field of organosilicon chemistry, as a reagent or a precursor for the synthesis of more complex molecules. Cyclohex-2-enyldiphenylsilane is also of interest in materials science due to its potential applications in the development of new materials with unique properties.

1829-51-2

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1829-51-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1829-51-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,8,2 and 9 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1829-51:
(6*1)+(5*8)+(4*2)+(3*9)+(2*5)+(1*1)=92
92 % 10 = 2
So 1829-51-2 is a valid CAS Registry Number.

1829-51-2Relevant academic research and scientific papers

Selective mono- and di-allylation and allenylation of chlorosilanes using indium

Li, Zhifang,Yang, Chenjun,Zheng, Hongfang,Qiu, Huayu,Lai, Guoqiao

scheme or table, p. 3771 - 3779 (2009/02/08)

Allyl and allenyl groups have been introduced into silicon systems by the allylation and allenylation of chlorosilanes using allyl bromide or propargyl bromide with indium. The allylation of chlorosilanes afforded a variety of aryl, aralkyl, and alkenyl substituted allylsilanes. By applying this method, the reactions of 1-bromo-3-methylbut-2-ene, 3-bromo-2-methylprop-1-ene and 3-bromobut-1-ene with chlorosilanes also proceed smoothly to give regioselectively allylic rearrangement products in good yields. Mediated by indium, dichlorosilanes (R2SiCl2) and trichlorosilanes (RSiCl3) can either afford monoallylated silanes or diallylated silanes depending on the amount of allyl bromide and indium used.

Group 6 anionic ·-hydride complexes [HM2(CO)10]- (M = Cr, Mo, W): New catalysts for hydrogenation and hydrosilylation

Fuchikami, Takamasa,Ubukata, Yumiko,Tanaka, Yasutaka

, p. 1199 - 1202 (2007/10/02)

Group 6 anionic ·-hydride complexes catalyze hydrogenation of conjugated olefins, aldehydes, ketoesters, and alkynes, and hydrosilylation of aldehydes and conjugated olefins with high regio- and stereoselectivity. Ketones are converted into silyl ethers and silyl enol ethers with monohydrosilanes and dihydrosilanes, respectively.

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