6-Fluoro-3-formylchromone
≥97%
- Product Code: 57062
CAS:
69155-76-6
| Molecular Weight: | 192.15 g./mol | Molecular Formula: | C₁₀H₅FO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00139060 | |
| Melting Point: | 157°C | Boiling Point: | |
| Density: | Storage Condition: | room temperature, dry |
Product Description:
6-Fluoro-3-formylchromone is primarily utilized in organic synthesis as a versatile intermediate for constructing complex molecules. Its structure, featuring both a formyl group and a fluorine atom, makes it valuable in the development of pharmaceuticals, particularly in the synthesis of chromone derivatives with potential biological activities. It is often employed in medicinal chemistry to create compounds that may exhibit anti-inflammatory, antimicrobial, or anticancer properties. Additionally, its reactive formyl group allows for further functionalization, enabling the preparation of heterocyclic compounds and other derivatives used in drug discovery and development. Its application extends to material science, where it serves as a building block for designing fluorescent dyes and other functional materials.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | Light yellow to yellow Solid |
| PURITY | 96.5-100 |
| Infrared spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | Ft5,925.76 |
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| 1.000 | 10-20 days | Ft14,545.05 |
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6-Fluoro-3-formylchromone
6-Fluoro-3-formylchromone is primarily utilized in organic synthesis as a versatile intermediate for constructing complex molecules. Its structure, featuring both a formyl group and a fluorine atom, makes it valuable in the development of pharmaceuticals, particularly in the synthesis of chromone derivatives with potential biological activities. It is often employed in medicinal chemistry to create compounds that may exhibit anti-inflammatory, antimicrobial, or anticancer properties. Additionally, its reactive formyl group allows for further functionalization, enabling the preparation of heterocyclic compounds and other derivatives used in drug discovery and development. Its application extends to material science, where it serves as a building block for designing fluorescent dyes and other functional materials.
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