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Bis(3-bromophenyl)dimethylsilane is a chemical compound with the molecular formula C16H16Br2Si. It is a silane compound that contains two brominated phenyl groups and two methyl groups attached to a silicon atom. It is a colorless liquid with a strong odor and is flammable.

151238-31-2

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151238-31-2 Usage

Uses

Used in Organic Synthesis:
Bis(3-bromophenyl)dimethylsilane is used as a reagent in organic synthesis for the formation of carbon-carbon and carbon-heteroatom bonds.
Used in Pharmaceutical Industry:
Bis(3-bromophenyl)dimethylsilane is used as a reagent in cross-coupling reactions to form complex organic molecules for drug development.
Used in Agrochemical Industry:
Bis(3-bromophenyl)dimethylsilane is used as a reagent in the synthesis of agrochemicals, such as pesticides and herbicides.
Used in Materials Science:
Bis(3-bromophenyl)dimethylsilane is used in the development of new materials with specific properties, such as polymers and coatings.

Check Digit Verification of cas no

The CAS Registry Mumber 151238-31-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,1,2,3 and 8 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 151238-31:
(8*1)+(7*5)+(6*1)+(5*2)+(4*3)+(3*8)+(2*3)+(1*1)=102
102 % 10 = 2
So 151238-31-2 is a valid CAS Registry Number.

151238-31-2SDS

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 bis(3-bromophenyl)dimethylsilane

1.2 Other means of identification

Product number -
Other names -

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:151238-31-2 SDS

151238-31-2Relevant academic research and scientific papers

POLYCYCLIC COMPOUND AND ORGANIC LIGHT-EMITTING DEVICE INCLUDING SAME

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Paragraph 0185-0186; 0298-0299, (2021/10/15)

A compound of Chemical Formula 1, and an organic light emitting device including the same.

Novel anthracene compound and organic light emitting device comprising the same

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Paragraph 0191-0194, (2020/09/16)

The present invention provides a novel anthracene compound and an organic light emitting device using the same, wherein the compound is represented by chemical formula 1.

COLORING COMPOSITION, INKJET INK, AND TEXTILE PRINTING METHOD

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Paragraph 0150; 0151; 0152, (2017/10/11)

PROBLEM TO BE SOLVED: To provide: a coloring composition excellent in cyan optical density (OD value) and light fastness, an inkjet ink containing the coloring composition, and a textile printing method using the coloring composition or the inkjet ink. SO

Synthesis and characterization of di-, tri- and tetraboronic acids based on phenyl- and thienylsilane cores

Gontarczyk, Krzysztof,Durka, Krzysztof,Klimkowski, Piotr,Luliński, Sergiusz,Serwatowski, Janusz,Wo?niak, Krzysztof

, p. 1 - 9 (2015/03/04)

The synthesis of a series of di- tri- and tetraboronic acids based on respective phenyl- and thienylsilane cores is described. The optimal protocols involved lithiation of respective arylsilane precursors using either deprotonative lithiation or halogen/lithium exchange with n-BuLi followed by treatment of resultant intermediates with B(Oi-Pr)3 and subsequent hydrolysis, which afforded final products in good yields. X-ray crystal structures of selected diboronic derivatives were determined showing that hydrogen-bonding interactions of B(OH)2 groups are the main factor governing the supramolecular assembly.

Tetrahedral silicon-based luminescent molecules: Synthesis and comparison of thermal and photophysical properties by various effect factors

Wang, Dengxu,Wang, Linlin,Xue, Lei,Zhou, Debo,Feng, Shengyu,Zhao, Xian

, p. 58 - 64 (2013/06/26)

A series of luminescent molecules were presented employing the tetrahedral structural motif of the silicon atom, which further connected different N-containing heterocycle functional groups in their periphery using phenyl rings as the bridges. These compounds included three kinds of N-heterocycle functional silanes: imidazole derivatives (1a-h), pyrazole derivatives (2a-e) and benzimidazole derivatives (3a-b), and their structures were fully characterized by FT-IR, 1H NMR, 13C NMR and HRMS. The TGA results indicate that they all exhibit high thermal stabilities. The photophysical properties demonstrate that they are fluorescent in the violet-blue region and could be potentially applied as blue emitters for organic light-emitting diodes (OLEDs). The effect factors of sort, disposition and number of substituent groups and N-containing heterocycle functional groups on their thermal and photophysical properties were investigated. Molecular calculations were also performed to support the experimental results. Moreover, the computational results reveal that these compounds all exhibit relatively large HOMO-LUMO band gaps with the range from 4.82 eV (2d) to 5.19 eV (1a and 2c), making them become promising candidates as host materials for emitters and hole/electron blocking materials in OLEDs display.

Magnetic interaction between two triplet nitrene units through diphenylsilane and 1,2-diphenyldisilane couplers

Doi, Takatsugu,Ichimura, Andrew S.,Koga, Noboru,Iwamura, Hiizu

, p. 8928 - 8932 (2007/10/02)

m,m′-,m,p′-, and p,p′-Bis(azidophenyl)dimethylsilanes 1a and 1,2-bis(azidophenyl)-1,1,2,2-tetramethyldisilanes 2a were prepared, and the dipolar and exchange couplings in the corresponding dinitrenes 1n and 2n generated photochemically were investigated b

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