2-Bromo-5-ethylthiophene
≥95%
- Product Code: 66796
CAS:
62323-44-8
| Molecular Weight: | 191.09 g./mol | Molecular Formula: | C₆H₇BrS |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD12033305 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, protected from light, stored under inert gas |
Product Description:
2-Bromo-5-ethylthiophene is primarily used in organic synthesis as a versatile building block for the development of more complex chemical structures. Its application is significant in the field of medicinal chemistry, where it serves as an intermediate in the synthesis of pharmaceutical compounds. The bromine atom in the molecule allows for further functionalization through cross-coupling reactions, such as Suzuki or Heck reactions, which are essential for creating diverse organic molecules.
In material science, this compound is utilized in the production of conductive polymers and organic semiconductors. Its thiophene ring structure is particularly valuable for constructing π-conjugated systems, which are crucial for electronic and optoelectronic devices like organic light-emitting diodes (OLEDs) and field-effect transistors (OFETs).
Additionally, 2-Bromo-5-ethylthiophene is employed in agrochemical research for the synthesis of novel pesticides and herbicides. Its chemical properties enable the creation of compounds that can interact with biological systems in specific ways, making it a useful tool in the development of crop protection agents.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.250 | 10-20 days | ฿270.00 |
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| 1.000 | 10-20 days | ฿531.00 |
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| 5.000 | 10-20 days | ฿2,574.00 |
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2-Bromo-5-ethylthiophene
2-Bromo-5-ethylthiophene is primarily used in organic synthesis as a versatile building block for the development of more complex chemical structures. Its application is significant in the field of medicinal chemistry, where it serves as an intermediate in the synthesis of pharmaceutical compounds. The bromine atom in the molecule allows for further functionalization through cross-coupling reactions, such as Suzuki or Heck reactions, which are essential for creating diverse organic molecules.
In material science, this compound is utilized in the production of conductive polymers and organic semiconductors. Its thiophene ring structure is particularly valuable for constructing π-conjugated systems, which are crucial for electronic and optoelectronic devices like organic light-emitting diodes (OLEDs) and field-effect transistors (OFETs).
Additionally, 2-Bromo-5-ethylthiophene is employed in agrochemical research for the synthesis of novel pesticides and herbicides. Its chemical properties enable the creation of compounds that can interact with biological systems in specific ways, making it a useful tool in the development of crop protection agents.
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