Methyl 2,5-difluoronicotinate
≥95%
- Product Code: 115390
CAS:
1214362-39-6
| Molecular Weight: | 173.12 g./mol | Molecular Formula: | C₇H₅F₂NO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD14698038 | |
| Melting Point: | Boiling Point: | 218.9±40.0°C at 760 mmHg | |
| Density: | Storage Condition: | room temperature, stored under inert gas |
Product Description:
Methyl 2,5-difluoronicotinate is primarily used as an intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Its structure, featuring fluorine atoms and a nicotinate moiety, makes it valuable for constructing complex molecules with enhanced biological activity. In medicinal chemistry, it serves as a building block for the synthesis of active pharmaceutical ingredients (APIs), especially those targeting central nervous system disorders or infectious diseases. Additionally, its fluorinated aromatic ring contributes to improved metabolic stability and bioavailability in drug candidates. In agrochemical research, it is utilized to develop novel pesticides or herbicides with higher efficacy and selectivity. The compound’s versatility in chemical reactions, such as cross-coupling or nucleophilic substitution, further expands its utility in industrial and academic research settings.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿2,718.00 |
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| 0.250 | 10-20 days | ฿4,617.00 |
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Methyl 2,5-difluoronicotinate
Methyl 2,5-difluoronicotinate is primarily used as an intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Its structure, featuring fluorine atoms and a nicotinate moiety, makes it valuable for constructing complex molecules with enhanced biological activity. In medicinal chemistry, it serves as a building block for the synthesis of active pharmaceutical ingredients (APIs), especially those targeting central nervous system disorders or infectious diseases. Additionally, its fluorinated aromatic ring contributes to improved metabolic stability and bioavailability in drug candidates. In agrochemical research, it is utilized to develop novel pesticides or herbicides with higher efficacy and selectivity. The compound’s versatility in chemical reactions, such as cross-coupling or nucleophilic substitution, further expands its utility in industrial and academic research settings.
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