1-Bromo-3-(trimethylsilyl)benzene

96%

Reagent Code: #88145
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CAS Number 17878-47-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 229.19 g/mol
Formula C₉H₁₃BrSi
badge Registry Numbers
MDL Number MFCD00093882
thermostat Physical Properties
Boiling Point 50°C/0.5mmHg(lit.)
inventory_2 Storage & Handling
Density 1.22g/ml
Storage room temperature, dry

description Product Description

This chemical is primarily used in organic synthesis as a versatile intermediate. It serves as a building block in the preparation of more complex organic compounds, particularly in the field of pharmaceuticals and materials science. The trimethylsilyl group acts as a protective group for sensitive functional groups during chemical reactions, allowing for selective transformations. Additionally, it is employed in cross-coupling reactions, such as Suzuki-Miyaura and Stille couplings, to create carbon-carbon bonds, which are essential in the synthesis of various organic molecules. Its bromine substituent makes it a suitable candidate for further functionalization through substitution reactions.

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Test Parameter Specification
Appearance White to Yellow Powder or Crystals
Purity 96.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿830.00
inventory 5g
10-20 days ฿2,440.00
1-Bromo-3-(trimethylsilyl)benzene
This chemical is primarily used in organic synthesis as a versatile intermediate. It serves as a building block in the preparation of more complex organic compounds, particularly in the field of pharmaceuticals and materials science. The trimethylsilyl group acts as a protective group for sensitive functional groups during chemical reactions, allowing for selective transformations. Additionally, it is employed in cross-coupling reactions, such as Suzuki-Miyaura and Stille couplings, to create carbon-carbon bonds, which are essential in the synthesis of various organic molecules. Its bromine substituent makes it a suitable candidate for further functionalization through substitution reactions.
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