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Postion:Product Catalog >Chemical Reagents>Organic reagents>Silane>Bromotrimethylsilane
Bromotrimethylsilane
  • Bromotrimethylsilane
  • Bromotrimethylsilane
  • Bromotrimethylsilane
  • Bromotrimethylsilane
  • Bromotrimethylsilane

Bromotrimethylsilane

Price Get Latest Price
Package 1kg
Min. Order: 1kg
Supply Ability: 20tons
Update Time: 2023-09-14

Product Details

Product Name: Bromotrimethylsilane CAS No.: 2857-97-8
EC-No.: 220-672-0 Min. Order: 1kg
Purity: 99.32% Supply Ability: 20tons
Release date: 2023/09/14

Application:


Bromotrimethylsilane is a chemical compound with the formula (CH3)3SiBr. Here are some possible applications of this compound:


1. It can be used as a reagent for the synthesis of various organosilicon compounds, such as siloxanes, silanes, and silazanes. The bromine atom can be replaced with other functional groups, such as alkyl, aryl, or acyl groups, to modify the properties of the resulting compounds.


2. It can be used as a protecting group for alcohols, amines, and carboxylic acids in organic synthesis. The trimethylsilyl (TMS) group is easily removable under mild conditions, allowing the desired functional group to be regenerated.


3. It can be used as a catalyst or co-catalyst in various organic reactions, such as Friedel-Crafts acylation and alkylation, hydrosilylation, and cross-coupling reactions. The TMS group can enhance the reactivity or selectivity of the catalyst, or stabilize reactive intermediates.


4. It can be used as a precursor for the synthesis of other functionalized silicon compounds, such as silicones, silsesquioxanes, and silafluorenes. The TMS group can serve as a building block or a protecting group in the synthesis of these compounds.


5. It can be used as a reagent for the analysis of various organic compounds, such as alcohols, amines, and carboxylic acids, by gas chromatography or mass spectrometry. The TMS group can enhance the volatility, stability, or detectability of the analyte.


Overall, bromotrimethylsilane is a versatile and useful compound in organic synthesis and materials science, due to its reactivity, stability, and compatibility with other functional groups.

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