4-Methoxy-2-(trifluoromethyl)pyridine
95%
- Product Code: 119466
CAS:
1065103-97-0
| Molecular Weight: | 177.12 g./mol | Molecular Formula: | C₇H₆F₃NO |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD11054356 | |
| Melting Point: | Boiling Point: | 170.8±40.0 °C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
This chemical is primarily utilized in the pharmaceutical and agrochemical industries as a key intermediate in the synthesis of various active compounds. Its unique structure, featuring a methoxy group and a trifluoromethyl group on a pyridine ring, makes it valuable for developing molecules with enhanced biological activity and stability. In pharmaceuticals, it is often employed in the creation of drugs targeting specific diseases, including anti-inflammatory and anti-cancer agents. In agrochemicals, it serves as a building block for designing pesticides and herbicides, leveraging its ability to improve the efficacy and selectivity of these products. Additionally, its trifluoromethyl group contributes to increased lipophilicity, which can enhance the bioavailability of the final compounds.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿3,825.00 |
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| 0.250 | 10-20 days | ฿6,489.00 |
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| 1.000 | 10-20 days | ฿17,514.00 |
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4-Methoxy-2-(trifluoromethyl)pyridine
This chemical is primarily utilized in the pharmaceutical and agrochemical industries as a key intermediate in the synthesis of various active compounds. Its unique structure, featuring a methoxy group and a trifluoromethyl group on a pyridine ring, makes it valuable for developing molecules with enhanced biological activity and stability. In pharmaceuticals, it is often employed in the creation of drugs targeting specific diseases, including anti-inflammatory and anti-cancer agents. In agrochemicals, it serves as a building block for designing pesticides and herbicides, leveraging its ability to improve the efficacy and selectivity of these products. Additionally, its trifluoromethyl group contributes to increased lipophilicity, which can enhance the bioavailability of the final compounds.
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