6-Methyl-4-(trifluoromethyl)pyridin-2-amine
97%
- Product Code: 50054
CAS:
165385-89-7
| Molecular Weight: | 176.1391 g./mol | Molecular Formula: | C₇H₇F₃N₂ |
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| EC Number: | MDL Number: | MFCD10697683 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This chemical is primarily utilized in the pharmaceutical and agrochemical industries due to its unique structural properties. In pharmaceuticals, it serves as a key intermediate in the synthesis of various active pharmaceutical ingredients (APIs), particularly those targeting central nervous system disorders and inflammatory diseases. Its trifluoromethyl group enhances the biological activity and metabolic stability of the resulting compounds.
In agrochemicals, it is employed in the development of pesticides and herbicides. The presence of the trifluoromethyl group contributes to the efficacy of these products by improving their ability to interact with biological targets in pests and weeds. Additionally, its pyridine ring structure is advantageous in creating compounds with specific modes of action, making it valuable in designing next-generation crop protection agents. Its versatility and effectiveness make it a crucial component in advancing both medicinal and agricultural chemical research.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.050 | 10-20 days | ฿9,009.00 |
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6-Methyl-4-(trifluoromethyl)pyridin-2-amine
This chemical is primarily utilized in the pharmaceutical and agrochemical industries due to its unique structural properties. In pharmaceuticals, it serves as a key intermediate in the synthesis of various active pharmaceutical ingredients (APIs), particularly those targeting central nervous system disorders and inflammatory diseases. Its trifluoromethyl group enhances the biological activity and metabolic stability of the resulting compounds.
In agrochemicals, it is employed in the development of pesticides and herbicides. The presence of the trifluoromethyl group contributes to the efficacy of these products by improving their ability to interact with biological targets in pests and weeds. Additionally, its pyridine ring structure is advantageous in creating compounds with specific modes of action, making it valuable in designing next-generation crop protection agents. Its versatility and effectiveness make it a crucial component in advancing both medicinal and agricultural chemical research.
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