(2-Chloro-3-fluoropyridin-4-yl)methanol
98%
- Product Code: 163308
CAS:
946127-54-4
| Molecular Weight: | 161.56 g./mol | Molecular Formula: | C₆H₅ClFNO |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD11045047 | |
| Melting Point: | Boiling Point: | 263.7±35.0 °C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, dry, sealed |
Product Description:
Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for creating analogs with improved potency and metabolic stability. Commonly employed in the preparation of agrochemicals and drug candidates targeting inflammatory and neurological disorders. The presence of both chlorine and fluorine atoms enhances binding affinity to target proteins, while the hydroxyl group enables further chemical modifications through esterification or ether formation.
Product Specification:
| Test | Specification |
|---|---|
| Appearance | White to Off-white Solid |
| Purity (%) | 97.5-100 |
| Infrared Spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 250mg | 10-20 days | $61.19 |
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| 1g | 10-20 days | $145.83 |
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| 5g | 10-20 days | $596.04 |
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(2-Chloro-3-fluoropyridin-4-yl)methanol
Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for creating analogs with improved potency and metabolic stability. Commonly employed in the preparation of agrochemicals and drug candidates targeting inflammatory and neurological disorders. The presence of both chlorine and fluorine atoms enhances binding affinity to target proteins, while the hydroxyl group enables further chemical modifications through esterification or ether formation.
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