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1,1-diphenyl-1,2,3,4-tetrahydrosiline is a unique organosilicon compound characterized by its molecular formula C16H18Si. 1,1‐diphenyl‐1,2,3,4‐tetrahydrosiline features a silicon atom at its core, bonded to four carbon atoms, with two phenyl groups (C6H5) attached to the silicon, and two additional carbon atoms forming a cyclohexane-like ring structure. The presence of the phenyl groups and the tetrahydrosiline ring gives 1,1‐diphenyl‐1,2,3,4‐tetrahydrosiline distinct chemical and physical properties, making it a subject of interest in the field of organosilicon chemistry. It is important to note that the compound's exact properties, such as reactivity, stability, and potential applications, would require further investigation and are not specified in this summary.

2736-08-5

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2736-08-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2736-08-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,7,3 and 6 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 2736-08:
(6*2)+(5*7)+(4*3)+(3*6)+(2*0)+(1*8)=85
85 % 10 = 5
So 2736-08-5 is a valid CAS Registry Number.

2736-08-5Relevant academic research and scientific papers

Nickel-catalyzed insertions of vinylidenes into Si-H bonds

Biswas, Sourish,Pal, Sudipta,Uyeda, Christopher

supporting information, p. 14175 - 14178 (2020/11/24)

A nickel-catalyzed reductive cyclization of 1,1-dichloroalkenyl silanes is reported. The products of this reaction are unsaturated five-or six-membered silacycles. Intermolecular variants are also described, providing access to trisubstituted vinyl silanes that are not accessible by alkyne hydrosilylation or sila-Heck-type processes. A variety of silanes can be utilized, including those that serve as nucleophilic partners in Hiyama cross-coupling reactions. Mechanistic studies using deuterium-labelled silanes are described. This journal is

Synthesis of unsaturated silyl heterocycles via an intramolecular silyl-heck reaction

Reid, William B.,McAtee, Jesse R.,Watson, Donald A.

, p. 3796 - 3803 (2019/10/11)

We report the synthesis of unsaturated silacycles via an intramolecular silyl-Heck reaction. Using palladium catalysis, silicon electrophiles tethered to alkenes cyclize to form five- and six-membered silicon heterocycles. The effects of alkene substitution and tether length on the efficiency and regioselectivity of the cyclizations are described. Finally, through the use of an intramolecular tether, the first examples of disubstituted alkenes in silyl-Heck reactions are reported.

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