3-Bromo-5-methylthiophene-2-carbaldehyde
97%
- Product Code: 45289
CAS:
36155-82-5
| Molecular Weight: | 205.0723 g./mol | Molecular Formula: | C₆H₅BrOS |
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| EC Number: | MDL Number: | MFCD01859869 | |
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| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in organic synthesis as a versatile intermediate for the development of complex molecules. It is often employed in the construction of heterocyclic compounds, particularly in the synthesis of thiophene derivatives, which are significant in pharmaceutical and agrochemical research. Its bromine and aldehyde functional groups make it a valuable building block for cross-coupling reactions, such as Suzuki or Sonogashira couplings, enabling the creation of diverse chemical structures. Additionally, it is used in the preparation of organic materials, including conductive polymers and dyes, due to the electron-rich nature of the thiophene ring. Its applications also extend to the field of medicinal chemistry, where it serves as a precursor for the development of biologically active molecules.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $76.62 |
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3-Bromo-5-methylthiophene-2-carbaldehyde
This compound is primarily utilized in organic synthesis as a versatile intermediate for the development of complex molecules. It is often employed in the construction of heterocyclic compounds, particularly in the synthesis of thiophene derivatives, which are significant in pharmaceutical and agrochemical research. Its bromine and aldehyde functional groups make it a valuable building block for cross-coupling reactions, such as Suzuki or Sonogashira couplings, enabling the creation of diverse chemical structures. Additionally, it is used in the preparation of organic materials, including conductive polymers and dyes, due to the electron-rich nature of the thiophene ring. Its applications also extend to the field of medicinal chemistry, where it serves as a precursor for the development of biologically active molecules.
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