2-Bromo-3-(bromomethyl)thiophene

96%

Reagent Code: #77140
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CAS Number 40032-76-6

science Other reagents with same CAS 40032-76-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 255.96 g/mol
Formula C₅H₄Br₂S
badge Registry Numbers
MDL Number MFCD02180908
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Storage room temperature

description Product Description

2-Bromo-3-(bromomethyl)thiophene is primarily used as a key intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Its reactive bromine sites make it valuable for constructing complex molecular structures through cross-coupling reactions, such as Suzuki or Heck reactions. This compound is also employed in the synthesis of thiophene-based polymers, which are essential materials in organic electronics, including organic light-emitting diodes (OLEDs) and organic field-effect transistors (OFETs). Additionally, it serves as a building block in the preparation of heterocyclic compounds, which are widely explored for their biological activities in medicinal chemistry.

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Test Parameter Specification
Appearance Colorless to brown liquid
Purity 95.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿3,090.00
inventory 5g
10-20 days ฿9,140.00

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2-Bromo-3-(bromomethyl)thiophene
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2-Bromo-3-(bromomethyl)thiophene is primarily used as a key intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Its reactive bromine sites make it valuable for constructing complex molecular structures through cross-coupling reactions, such as Suzuki or Heck reactions. This compound is also employed in the synthesis of thiophene-based polymers, which are essential materials in organic electronics, including organic light-emitting diodes (OLEDs) and org

2-Bromo-3-(bromomethyl)thiophene is primarily used as a key intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Its reactive bromine sites make it valuable for constructing complex molecular structures through cross-coupling reactions, such as Suzuki or Heck reactions. This compound is also employed in the synthesis of thiophene-based polymers, which are essential materials in organic electronics, including organic light-emitting diodes (OLEDs) and organic field-effect transistors (OFETs). Additionally, it serves as a building block in the preparation of heterocyclic compounds, which are widely explored for their biological activities in medicinal chemistry.

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