2,3,5-Tribromo-4-methylthiophene
≥95%
- Product Code: 240255
CAS:
67869-13-0
| Molecular Weight: | 334.85 g./mol | Molecular Formula: | C₅H₃Br₃S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00130086 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, avoiding light |
Product Description:
Used primarily as an intermediate in the synthesis of pharmaceuticals and agrochemicals, this compound serves as a building block in heterocyclic chemistry due to the presence of multiple bromine atoms and a thiophene ring. The bromine substituents allow for further functionalization via cross-coupling reactions such as Suzuki or Heck reactions, enabling the construction of complex organic molecules. It is also employed in the development of organic semiconductors and electronic materials, where brominated thiophene derivatives help tune electronic properties and improve material stability. Additionally, it finds use in research settings for the preparation of ligands and catalysts in transition metal-mediated transformations.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 5.000 | 10-20 days | ฿1,010.00 |
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| 25.000 | 10-20 days | ฿4,630.00 |
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2,3,5-Tribromo-4-methylthiophene
Used primarily as an intermediate in the synthesis of pharmaceuticals and agrochemicals, this compound serves as a building block in heterocyclic chemistry due to the presence of multiple bromine atoms and a thiophene ring. The bromine substituents allow for further functionalization via cross-coupling reactions such as Suzuki or Heck reactions, enabling the construction of complex organic molecules. It is also employed in the development of organic semiconductors and electronic materials, where brominated thiophene derivatives help tune electronic properties and improve material stability. Additionally, it finds use in research settings for the preparation of ligands and catalysts in transition metal-mediated transformations.
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