2-Bromo-3-(bromomethyl)thiophene
96%
- Product Code: 77140
CAS:
40032-76-6
| Molecular Weight: | 255.96 g./mol | Molecular Formula: | C₅H₄Br₂S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD02180908 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
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.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | Colorless to Brown Liquid |
| PURITY | 95.5-100 |
| Infrared spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿3,090.00 |
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| 5.000 | 10-20 days | ฿9,140.00 |
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2-Bromo-3-(bromomethyl)thiophene
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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