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1-BROMO-3-TRIMETHYLSILYLBENZENE is an organosilicon compound that serves as a versatile building block in organic synthesis. It is a benzene derivative characterized by the presence of a bromine atom at the 1-position and a trimethylsilyl group at the 3-position. 1-BROMO-3-TRIMETHYLSILYLBENZENE is known for its reactivity and versatility, making it a valuable asset in the realms of organic chemistry and materials science.

17878-47-6

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17878-47-6 Usage

Uses

Used in Organic Synthesis:
1-BROMO-3-TRIMETHYLSILYLBENZENE is used as a reagent in cross-coupling reactions for the formation of carbon-carbon bonds. Its unique structure allows for the creation of new compounds with potential applications in various fields.
Used in Pharmaceutical and Agrochemical Industries:
In the pharmaceutical and agrochemical sectors, 1-BROMO-3-TRIMETHYLSILYLBENZENE is utilized as a key intermediate in the synthesis of a wide range of active ingredients. Its ability to form carbon-carbon bonds makes it instrumental in the development of new drugs and pesticides.
Used in the Production of Functional Materials and Polymers:
1-BROMO-3-TRIMETHYLSILYLBENZENE also serves as a precursor in the synthesis of functional materials and polymers. Its incorporation into these materials can enhance their properties, such as stability, reactivity, or specific chemical functionalities, depending on the desired application.
Overall, 1-BROMO-3-TRIMETHYLSILYLBENZENE's diverse applications across different industries highlight its importance as a synthetic building block and a precursor for creating innovative materials and compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 17878-47-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,8,7 and 8 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 17878-47:
(7*1)+(6*7)+(5*8)+(4*7)+(3*8)+(2*4)+(1*7)=156
156 % 10 = 6
So 17878-47-6 is a valid CAS Registry Number.
InChI:InChI=1/C9H13BrSi/c1-11(2,3)9-6-4-5-8(10)7-9/h4-7H,1-3H3

17878-47-6Relevant articles and documents

Synthesis, radiosynthesis, and biological evaluation of carbon-11 labeled 2β-carbomethoxy-3β-(3′-((Z)-2-haloethenyl)phenyl)nortropanes: Candidate radioligands for in vivo imaging of the serotonin transporter with positron emission tomography

Stehouwer, Jeffrey S.,Jarkas, Nachwa,Zeng, Fanxing,Voll, Ronald J.,Williams, Larry,Owens, Michael J.,Votaw, John R.,Goodman, Mark M.

, p. 6760 - 6767 (2006)

2β-Carbomethoxy-3β-(3′-((Z)-2-iodoethenyl)phenyl)nortropane (mZIENT, 1) and 2β-carbomethoxy-3β-(3′-((Z)-2-bromoethenyl) phenyl)nortropane (mZBrENT, 2) were synthesized and evaluated for binding to the human serotonin, dopamine, and norepinephrine transpor

Oxidative 1,2-Difunctionalization of Ethylene via Gold-Catalyzed Oxyarylation

Harper, Matthew J.,Emmett, Edward J.,Bower, John F.,Russell, Christopher A.

supporting information, p. 12386 - 12389 (2017/09/22)

Under the conditions of oxidative gold catalysis, exposure of ethylene to aryl silanes and alcohols generates products of 1,2-oxyarylation. This provides a rare example of a process that allows catalytic differential 1,2-difunctionalization of this feedstock chemical.

Oxidative homocoupling reaction of aryltrimethylsilanes by Pd/o-chloranil catalysis

Shibata, Mari,Ito, Hideto,Itami, Kenichiro

supporting information, p. 1701 - 1704 (2017/11/23)

A practical oxidative homocoupling reaction of aryltri-methylsilanes has been achieved by Pd/o-chloranil catalytic system. The reaction shows the good functional group tolerability toward bromo, fluoro, ester, and methoxy groups to give a series of biaryls bearing electron-withdrawing and -donating groups. The boronate group is also retained on biaryls without any ArB bond cleavage, which is highly advantageous for orthogonal coupling.

Effect of silylated triarylphosphine ligands on rhodium-catalyzed hydrosilylation

Li, Jiayun,Xue, Mei,Bai, Ying,Peng, Jiajian,Xiao, Wenjun

, p. 905 - 910 (2016/10/18)

A series of silylated triarylphosphines was synthesized. Hydrosilylation reactions of styrene with triethoxysilane catalyzed by RhCl3/silylated triarylphosphine complexes were investigated. The complexes RhCl3/phenylbis(4-trimethylsilylphenyl)phosphine and RhCl3/tris(4-trimethylsilylphenyl)phosphine exhibited higher activity as well as greater β-adduct selectivity, and no unsaturated product was obtained. The results suggest that the silyl moieties have a significant impact on the catalytic process. Copyright

cis-Cinnamic acid selective suppressors distinct from auxin inhibitors

Okuda, Katsuhiro,Nishikawa, Keisuke,Fukuda, Hiroshi,Fujii, Yoshiharu,Shindo, Mitsuru

, p. 600 - 607 (2014/07/08)

The activity of cis-cinnamic acid (cis-CA), one of the allelochemicals, in plants is very similar to that of indole-3-acetic acid (IAA), a natural auxin, and thus cis-CA has long been believed to be an analog of auxin. We have reported some structure-acti

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.

DERIVATIVES OF INDOLE-2-CARBOXAMIDES AND OF AZAINDOLE-2-CARBOXAMIDES SUBSTITUTED WITH A SILANYL GROUP, PREPARATION THEREOF AND THERAPEUTIC USE THEREOF

-

Page/Page column 12, (2011/02/15)

This disclosure relates to compounds of formula (I): wherein G1, G2, G3, G4, n, Y, Z, Z1, Z2, Z3, and Z4 are as defined in the disclosure, or a salt thereof, or a hydr

AZABICYCLIC CARBOXAMIDE DERIVATIVES, PREPARATION THEREOF AND THERAPEUTIC USE THEREOF

-

Page/Page column 14, (2011/02/15)

The disclosure relates to compounds of formula (I): wherein X1, X2, X3, X4, Z1, Z2, Z3, Z4, Ra, Rb, n, Y, and W are as defined in the disclosure, or a salt thereof, or

BICYCLIC DERIVATIVES OF AZABICYCLIC CARBOXAMIDES, PREPARATION THEREOF AND THERAPEUTIC USE THEREOF

-

Page/Page column 16, (2011/02/15)

The disclosure relates to compounds of formula (I): wherein X1, X2, X3, X4, Y, n, A, and W are as defined in the disclosure, or a salt thereof, or a hydrate or solvate thereof, and to processes for the preparation of these compounds and the therapeutic use thereof.

Synthesis and gas permeation properties of various Si-containing poly(diarylacetylene)s and their desilylated membranes

Hu, Yanming,Hattori, Kyohei,Fukui, Akito,Shiotsuki, Masashi,Sanda, Fumio,Masuda, Toshio

scheme or table, p. 1548 - 1554 (2011/04/15)

Diarylacetylene monomers having trimethylsilyl groups and other substituents (substituted biphenyl, 1a and 1b; trimethylsilylmethylphenyl, 1c-e) were synthesized and polymerized with TaCl5-n-Bu4Sn catalyst to produce the correspondin

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