3-bromo-5-fluorobenzaldehyde
95%
- Product Code: 66307
CAS:
188813-02-7
| Molecular Weight: | 203.01 g./mol | Molecular Formula: | C₇H₄BrFO |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD04116319 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
3-bromo-5-fluorobenzaldehyde is primarily used in organic synthesis as a key intermediate for the production of various pharmaceuticals and agrochemicals. Its unique structure, featuring both bromine and fluorine substituents, makes it valuable in the development of complex molecules. It is often employed in cross-coupling reactions, such as Suzuki or Sonogashira couplings, to create biologically active compounds. Additionally, it serves as a building block in the synthesis of heterocyclic compounds, which are essential in drug discovery. The presence of the aldehyde group allows for further functionalization, enabling the creation of diverse chemical entities. This compound is particularly useful in medicinal chemistry for designing molecules with potential therapeutic applications.
Product Specification:
| Test | Specification |
|---|---|
| PUITY | 94.5-100 |
| APPEARANCE | OFF-WHITE TO YELLOW SOLID |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | £9.50 |
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| 5.000 | 10-20 days | £37.54 |
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| 25.000 | 10-20 days | £141.58 |
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| 100.000 | 10-20 days | £413.44 |
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3-bromo-5-fluorobenzaldehyde
3-bromo-5-fluorobenzaldehyde is primarily used in organic synthesis as a key intermediate for the production of various pharmaceuticals and agrochemicals. Its unique structure, featuring both bromine and fluorine substituents, makes it valuable in the development of complex molecules. It is often employed in cross-coupling reactions, such as Suzuki or Sonogashira couplings, to create biologically active compounds. Additionally, it serves as a building block in the synthesis of heterocyclic compounds, which are essential in drug discovery. The presence of the aldehyde group allows for further functionalization, enabling the creation of diverse chemical entities. This compound is particularly useful in medicinal chemistry for designing molecules with potential therapeutic applications.
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