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1-methyl-1-phenylsiletane is an organosilicon compound with the chemical formula C13H14Si. It is a colorless liquid at room temperature and is characterized by the presence of a silicon atom bonded to a methyl group and a phenyl group. 1-methyl-1-phenylsiletane is a derivative of siletane, which is a cyclic compound with silicon and carbon atoms in an alternating arrangement. 1-methyl-1-phenylsiletane is synthesized through various methods, including the reaction of phenylmagnesium bromide with chloromethylsilane. It is used in the synthesis of other organosilicon compounds and as a precursor in the production of silicones and other silicon-based materials. Due to its stability and unique properties, it has potential applications in the fields of materials science, pharmaceuticals, and chemical research.

3944-08-9

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3944-08-9 Usage

Explanation

The compound consists of 9 carbon atoms, 14 hydrogen atoms, and 1 silicon atom.

Explanation

It is a silicon-containing compound that forms a part of the larger group of organosilicon compounds.

Explanation

The compound appears as a colorless liquid at room temperature.

Explanation

1-methyl-1-phenylsiletane serves as a starting material for the production of various other organosilicon compounds.

Explanation

The compound is used in the fields of organic and materials chemistry for the development and study of new compounds and materials.

Explanation

The unique chemical structure of 1-methyl-1-phenylsiletane results in interesting chemical and physical properties, making it valuable for research and industrial purposes.

Explanation

Due to its unique properties, 1-methyl-1-phenylsiletane has potential applications in the pharmaceutical industry and as a reagent in organic synthesis processes.

Class

Organosilicon compounds

Physical state

Colorless liquid

Usage

Precursor in synthesis of other organosilicon compounds

Applications

Organic and materials chemistry

Chemical and physical properties

Unique and interesting

Potential applications

Pharmaceutical industry and as a reagent in organic synthesis

Check Digit Verification of cas no

The CAS Registry Mumber 3944-08-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,9,4 and 4 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 3944-08:
(6*3)+(5*9)+(4*4)+(3*4)+(2*0)+(1*8)=99
99 % 10 = 9
So 3944-08-9 is a valid CAS Registry Number.

3944-08-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-methyl-1-phenylsiletane

1.2 Other means of identification

Product number -
Other names 1-methyl-1-phenylsilacyclobutane

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:3944-08-9 SDS

3944-08-9Relevant academic research and scientific papers

Rhodium-Catalyzed Reaction of Silacyclobutanes with Unactivated Alkynes to Afford Silacyclohexenes

Chen, Hua,Chen, Yi,Tang, Xiaoxiao,Liu, Shunfa,Wang, Runping,Hu, Tianbao,Gao, Lu,Song, Zhenlei

supporting information, p. 4695 - 4699 (2019/03/07)

A Rh-catalyzed reaction of silacyclobutanes (SCBs) with unactivated alkynes has been developed to form silacyclohexenes with high chemoselectivity. Good enantioselectivity at the stereogenic silicon center was achieved using a chiral phosphoramidite ligand. The resulting silacyclohexenes are useful scaffolds for synthesizing structurally attractive silacyclic compounds.

Palladium-catalyzed desymmetrization of silacyclobutanes with alkynes: Enantioselective synthesis of silicon-stereogenic 1-sila-2-cyclohexenes and mechanistic considerations

Shintani, Ryo,Moriya, Kohei,Hayashi, Tamio

, p. 2902 - 2905 (2012/07/17)

A palladium-catalyzed enantioselective desymmetrization of silacyclobutanes with alkynes has been developed to give silicon-stereogenic 1-sila-2-cyclohexenes with high enantioselectivity. The products thus obtained undergo further derivatizations with complete stereoselectivity, and a new catalytic cycle involving alkyne coordination (oxidative cyclization)- transmetalation (σ-bond metathesis)-reductive elimination has also been proposed.

Synthesis of sodium-polystyrenesulfonate-grafted nanoparticles by core-cross-linking of block copolymer micelles

Matsumoto, Kozo,Hasegawa, Hirohiko,Matsuoka, Hideki

, p. 7197 - 7204 (2007/10/03)

Sodium poly(styrenesulfonate)(polySSNa)-grafted polymer nanoparticles were synthesized by core-cross-linking of block copolymer micelles and subsequent chemical transformation. Block copolymers, poly(p-((1-methyl)silacyclobutyl) styrene-block-poly(neopent

SILAETHENE I. DARSTELLUNG UND CHARAKTERISIERUNG VON MONOSILACYCLOBUTANEN

Auner, N.,Grobe, J.

, p. 25 - 52 (2007/10/02)

Monosilacyclobutanes of the type RR' are prepared by ring closure reactions of 3-halopropylhalosilanes and by substitution of SiCl containing silacyclobutane rings with organometallic reagents (RMgX, LiR, NaCp).Under optimal experimental conditions yields between 50 and 95percent can be obtained by both procedures.Characterization of the compounds is accomplished by analytical (C, H, N) and NMR, IR and mass spectroscopic investigations.

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