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Trisilane, 1,1,1,3,3,3-hexamethyl-2,2-bis(2,4,6-trimethylphenyl)-, also known as 1,1,1,3,3,3-hexamethyl-2,2-bis(2,4,6-trimethylphenyl)trisilane, is a complex organosilicon compound with the chemical formula C24H36Si3. Trisilane, 1,1,1,3,3,3-hexamethyl-2,2-bis(2,4,6-trimethylphenyl)- is characterized by its unique structure, which includes three methyl groups attached to each silicon atom, and two 2,4,6-trimethylphenyl groups bonded to the central carbon atom. It is a colorless, viscous liquid with a high boiling point and is insoluble in water. Due to its stability and unique properties, Trisilane, 1,1,1,3,3,3-hexamethyl-2,2-bis(2,4,6-trimethylphenyl)- has potential applications in the synthesis of various organosilicon materials and as a precursor in the production of silicone-based polymers.

79184-72-8

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79184-72-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 79184-72-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,1,8 and 4 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 79184-72:
(7*7)+(6*9)+(5*1)+(4*8)+(3*4)+(2*7)+(1*2)=168
168 % 10 = 8
So 79184-72-8 is a valid CAS Registry Number.

79184-72-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name bis(2,4,6-trimethylphenyl)-bis(trimethylsilyl)silane

1.2 Other means of identification

Product number -
Other names Mes2Si(SiMe3)2

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:79184-72-8 SDS

79184-72-8Relevant academic research and scientific papers

Electroreductive synthesis of some functionalized polysilanes and related polymers

Kashimura, Shigenori,Ishifune, Manabu,Bu, Hang-Bom,Takebayashi, Masakatsu,Kitajima, Satsuki,Yoshihara, Daisuke,Nishida, Ryoichi,Kawasaki, Shin-Ichi,Murase, Hiroaki,Shono, Tatsuya

, p. 4607 - 4610 (1997)

Polysilanes having hydroxyl and related Functional groups have been synthesized by the electroreduction of appropriate dichlorosilanes with Mg electrode, and a vinyl polymer which has oligosilane unit in the side chain has also been synthesized.

Electroreductive Synthesis of Polysilanes, Polygermanes, and Related Polymers with Magnesium Electrodes

Kashimura, Shigenori,Ishifune, Manabu,Yamashita, Natsuki,Bu, Hang-Bom,Takebayashi, Masakatsu,Kitajima, Satsuki,Yoshiwara, Daisuke,Kataoka, Yasuki,Nishida, Ryoichi,Kawasaki, Shin-Ichi,Murase, Hiroaki,Shono, Tatsuya

, p. 6615 - 6621 (2007/10/03)

The electroreduction of alkylaryldichlorosilane carried out with Mg cathode and anode in a single compartment cell gave high molecular weight poly(alkylarylsilane) (Mn = 5200-31000, Mw/Mn = 1.4-1.8) in 5-79% yield. The effects of electrode material, monomer concentration, amount of supplied electricity, and ultrasound were investigated. This electroreductive method was also successfully applied to the synthesis of polygermanes, silane-geramane copolymers, and also poly[p-(disilanylene)phenylenes].

Silicon-Carbon Unsaturated Compounds. 20. Formation and Reactions of Disilacyclopropanes and Molecular Structure of 3-(Hydroxydimesitylsilyl)-1,1-dimesityl-2,2-bis(trimethylsilyl)-1-silacyclopropane

Ishikawa, Mitsuo,Matsuzawa, Shigeji,Sugisawa, Hiroshi,Yano, Fujio,Kamitori, Shigehiro,Higuchi, Taiichi

, p. 7706 - 7710 (2007/10/02)

Two stable disilacyclopropanes, 1,1,2,2-tetramesityl-3-- and 1,1,2,2-tetramesityl-3--1,2-disilacyclopropane (3 and 8), have been prepared by addition of dimesitylsilylene to 1,1-dimesityl-3-ph

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