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6999-03-7

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6999-03-7 Usage

General Description

1-Bromo-4-trimethylsilylbenzene, also known as 4-(trimethylsilyl)phenyl bromide, is a chemical compound with the molecular formula C10H13BrSi. It is a relatively stable organic compound used as a reagent in various chemical reactions, particularly in organic synthesis. It has a molecular weight of 243.1 g/mol. It features a bromine atom linked to a benzene ring, which also bears a trimethylsilyl group. Safety data suggests that it is harmful if swallowed, inhaled, or comes into skin contact, and thus should be handled with proper protection. Its exact physical properties such as melting point, boiling point, and density can vary due to manufacturing conditions and impurities.

Check Digit Verification of cas no

The CAS Registry Mumber 6999-03-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,9 and 9 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 6999-03:
(6*6)+(5*9)+(4*9)+(3*9)+(2*0)+(1*3)=147
147 % 10 = 7
So 6999-03-7 is a valid CAS Registry Number.
InChI:InChI=1/C9H13BrSi/c1-11(2,3)9-6-4-8(10)5-7-9/h4-7H,1-3H3

6999-03-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name (4-Bromophenyl)trimethylsilane

1.2 Other means of identification

Product number -
Other names (4-bromophenyl)-trimethylsilane

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:6999-03-7 SDS

6999-03-7Relevant articles and documents

Synthesis of new monofunctional organosilicon molecules - Prospective efficient stoppers for the design of new siloxane polymers of unusual architecture

Anisimov, Anton A.,Kononevich, Yuriy N.,Korlyukov, Alexander A.,Arkhipov, Dmitry E.,Kononova, Elena G.,Peregudov, Alexander S.,Shchegolikhina, Olga I.,Muzafarov, Aziz M.

, p. 79 - 83 (2014)

The work reports the synthesis and characterization of new previously unknown bulk polyfunctional organosilanes with rigid molecular structure. The molecular structures of compounds 3 and 4 were defined by X-ray data. The possibility of use of prepared co

Orthogonal Stability and Reactivity of Aryl Germanes Enables Rapid and Selective (Multi)Halogenations

Deckers, Kristina,Fricke, Christoph,Schoenebeck, Franziska

supporting information, p. 18717 - 18722 (2020/08/25)

While halogenation is of key importance in synthesis and radioimaging, the currently available repertoire is largely designed to introduce a single halogen per molecule. This report makes the selective introduction of several different halogens accessible. Showcased here is the privileged stability of nontoxic aryl germanes under harsh fluorination conditions (that allow selective fluorination in their presence), while displaying superior reactivity and functional-group tolerance in electrophilic iodinations and brominations, outcompeting silanes or boronic esters under rapid and additive-free conditions. Mechanistic experiments and computational studies suggest a concerted electrophilic aromatic substitution as the underlying mechanism.

Design, synthesis and acaricidal activities of Cyflumetofen analogues based on carbon-silicon isosteric replacement

Beadle, Ryan,Cheng, Jiagao,Earley, Fergus G.,Li, Zhong,Maienfisch, Peter,Zhou, Cong

, (2020/04/30)

The application of a carbon-silicon bioisosteric replacement strategy to find new acaricides with improved properties led to the discovery of Sila-Cyflumetofen 6B, a novel and highly potent acaricide. The essential t-butyl group in the beta-ketonitrile ac

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