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Trisilane, also known as 1,1,1,3,3,3-hexamethyl-2-(2,4,6-trimethylphenyl)-2-(trimethylsilyl), is a complex organosilicon compound characterized by its unique structure. It features a central silicon atom bonded to three methyl groups and a phenyl ring, which is itself substituted with three methyl groups at the 2, 4, and 6 positions. Additionally, the phenyl ring is connected to a trimethylsilyl group, which further extends the molecule's complexity. Trisilane, 1,1,1,3,3,3-hexamethyl-2-(2,4,6-trimethylphenyl)-2-(trimethylsilyl)- is of interest in the field of organosilicon chemistry due to its potential applications in materials science and as a precursor in the synthesis of more complex silicon-containing molecules.

83241-99-0

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83241-99-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 83241-99-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,2,4 and 1 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 83241-99:
(7*8)+(6*3)+(5*2)+(4*4)+(3*1)+(2*9)+(1*9)=130
130 % 10 = 0
So 83241-99-0 is a valid CAS Registry Number.

83241-99-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-mesityl-2-(trimethylsilyl)hexamethyltrisilane

1.2 Other means of identification

Product number -
Other names tris-(trimethylsilyl)mesitylsilane

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:83241-99-0 SDS

83241-99-0Upstream product

83241-99-0Downstream Products

83241-99-0Relevant academic research and scientific papers

PHOTOLYSIS OF ORGANOPOLYSILANES. THE REACTION OF SILYLENES WITH ALLYL ETHYL ETHER

Ishikawa, Mitsuo,Katayama, Seiji,Kumada, Makoto

, p. 251 - 260 (2007/10/02)

The reactions of photochemically generated dimethylsilylene, methylphenylsilylene, phenyl(trimethylsilyl)silylene, and mesityl(trimethylsilyl)silylene with allyl ethyl ether have been investigated.Irradiation of dodecamethylcyclohexasilane in the presence of allyl ethyl ether at 10 deg C afforded 2-ethoxy-1,1-dimethyl-1-silacyclopropane, while similar photolysis at 35 deg C gave allylethoxydimethylsilane.The reaction of methylphenylsilylene and phenyl(trimethylsilyl)silylene at 10 deg C gave the respective silacyclopropanes, but at high temperature afforded the corresponding rearranged allylic silane derivatives.The photolysis of tris(trimethylsilyl)mesitylsilane in the presence of allyl ethyl ether resulted in formation of thermally stable 2-ethoxymethyl-1-mesityl-1-trimethylsilyl-1-silacyclopropane which did not afford the rearranged allylethoxydisilane at 200 deg C.

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