3-Bromo-4-iodothiophene
95%
- Product Code: 118012
CAS:
73882-41-4
| Molecular Weight: | 288.93 g./mol | Molecular Formula: | C₄H₂BrIS |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD18382466 | |
| Melting Point: | Boiling Point: | 107110°C at 3.5 mmHg | |
| Density: | Storage Condition: | 2-8°C, dry and sealed away from light |
Product Description:
This chemical is primarily used in organic synthesis, particularly in the development of complex thiophene derivatives. Its structure, featuring both bromine and iodine substituents, makes it a versatile intermediate in cross-coupling reactions, such as Suzuki or Sonogashira couplings, which are essential for creating advanced materials. It is also employed in the synthesis of conjugated polymers and small molecules for use in organic electronics, including organic light-emitting diodes (OLEDs) and organic photovoltaics (OPVs). Additionally, it serves as a building block in medicinal chemistry for the design of bioactive compounds and pharmaceuticals. Its unique reactivity allows for selective modifications, enabling researchers to tailor properties for specific applications in material science and drug discovery.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.100 | 10-20 days | $142.02 |
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| 0.250 | 10-20 days | $248.11 |
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| 1.000 | 10-20 days | $619.22 |
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3-Bromo-4-iodothiophene
This chemical is primarily used in organic synthesis, particularly in the development of complex thiophene derivatives. Its structure, featuring both bromine and iodine substituents, makes it a versatile intermediate in cross-coupling reactions, such as Suzuki or Sonogashira couplings, which are essential for creating advanced materials. It is also employed in the synthesis of conjugated polymers and small molecules for use in organic electronics, including organic light-emitting diodes (OLEDs) and organic photovoltaics (OPVs). Additionally, it serves as a building block in medicinal chemistry for the design of bioactive compounds and pharmaceuticals. Its unique reactivity allows for selective modifications, enabling researchers to tailor properties for specific applications in material science and drug discovery.
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