(Z)-4-Fluoro-N-hydroxybenzimidoyl chloride
97%
- Product Code: 246789
CAS:
393165-20-3
| Molecular Weight: | 173.57 g./mol | Molecular Formula: | C₇H₅ClFNO |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD02179417 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | -20°C, light-proof, inert gas |
Product Description:
Used primarily as an intermediate in the synthesis of fluorinated pharmaceuticals and agrochemicals. Its hydroxylamine-derived structure makes it suitable for constructing heterocyclic compounds, particularly in the development of bioactive molecules with antifungal, antibacterial, or anti-inflammatory properties. Commonly employed in condensation reactions to form oxadiazoles and other nitrogen-oxygen containing rings, which are key motifs in medicinal chemistry. Also utilized in the preparation of enzyme inhibitors where the Z-configuration around the imidoyl bond is critical for biological activity. Its reactivity allows for selective derivatization in multi-step organic syntheses, especially in routes requiring fluorinated aromatic building blocks.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 25.000 | 10-20 days | £893.13 |
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(Z)-4-Fluoro-N-hydroxybenzimidoyl chloride
Used primarily as an intermediate in the synthesis of fluorinated pharmaceuticals and agrochemicals. Its hydroxylamine-derived structure makes it suitable for constructing heterocyclic compounds, particularly in the development of bioactive molecules with antifungal, antibacterial, or anti-inflammatory properties. Commonly employed in condensation reactions to form oxadiazoles and other nitrogen-oxygen containing rings, which are key motifs in medicinal chemistry. Also utilized in the preparation of enzyme inhibitors where the Z-configuration around the imidoyl bond is critical for biological activity. Its reactivity allows for selective derivatization in multi-step organic syntheses, especially in routes requiring fluorinated aromatic building blocks.
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