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Trimethyl(3-methyl-2-phenylbut-2-en-1-yl)silane is an organosilicon compound characterized by a unique structure that combines a silicon atom with three methyl groups and a 3-methyl-2-phenylbut-2-en-1-yl group. This molecule features a phenyl ring attached to a butenyl chain, which is further substituted with a methyl group at the third carbon. The presence of the phenyl group and the unsaturated butenyl chain contribute to its chemical reactivity and potential applications in organic synthesis, particularly in reactions involving silicon-based reagents. The compound's structure also suggests that it may be used in the formation of silyl ethers or as a protecting group in organic synthesis, taking advantage of the stability and reactivity of silicon-based compounds.

66535-07-7

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66535-07-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 66535-07-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,5,3 and 5 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 66535-07:
(7*6)+(6*6)+(5*5)+(4*3)+(3*5)+(2*0)+(1*7)=137
137 % 10 = 7
So 66535-07-7 is a valid CAS Registry Number.

66535-07-7Downstream Products

66535-07-7Relevant academic research and scientific papers

Carbosilylation of allenes catalyzed by palladium complexes: A new efficient route to substituted allylic silanes

Wu,Yang,Cheng

, p. 2471 - 2474 (1999)

An aromatic or olefinic halide RX (C6H5I, p-CH3COC6H4I, p- NO2C6H4I, p-CH3OC6H4I, o-CH3OC6H4I, m-Csu

Nickel catalyzed dealkoxylative Csp2-Csp3 cross coupling reactions - Stereospecific synthesis of allylsilanes from enol ethers

Guo, Lin,Leiendecker, Matthias,Hsiao, Chien-Chi,Baumann, Christoph,Rueping, Magnus

supporting information, p. 1937 - 1940 (2015/02/05)

The application of cyclic and acyclic enol ethers as electrophiles in cross coupling reactions offers new possibilities for the preparation of functional compounds. A novel nickel catalyzed dealkoxylative cross coupling reaction allows access to structurally diverse allylsilanes and alcohol derivatives with high stereospecificity and in good yields under mild reaction conditions directly from the corresponding enol ethers.

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