(6-Chloro-5-(trifluoromethyl)pyridin-3-yl)methanol
97%
- Product Code: 57372
CAS:
1113049-91-4
Molecular Weight: | 211.57 g./mol | Molecular Formula: | C₇H₅ClF₃NO |
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EC Number: | MDL Number: | MFCD12024295 | |
Melting Point: | Boiling Point: | 269.4±35.0 °C at 760 mmHg | |
Density: | Storage Condition: | 2-8°C, store under inert gas |
Product Description:
(6-Chloro-5-(trifluoromethyl)pyridin-3-yl)methanol is primarily used as an intermediate in the synthesis of agrochemicals and pharmaceuticals. Its structure, featuring a trifluoromethyl group and a chloro substituent, makes it valuable in the development of compounds with enhanced biological activity. In agrochemicals, it is utilized in the production of herbicides and pesticides, where the trifluoromethyl group contributes to improved efficacy and stability. In the pharmaceutical industry, it serves as a building block for the creation of active pharmaceutical ingredients (APIs), particularly in the design of molecules targeting specific enzymes or receptors. Its versatility in chemical reactions allows for the creation of diverse derivatives, expanding its application in drug discovery and crop protection.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.100 | 10-20 days | $283.15 |
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0.250 | 10-20 days | $414.10 |
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(6-Chloro-5-(trifluoromethyl)pyridin-3-yl)methanol
(6-Chloro-5-(trifluoromethyl)pyridin-3-yl)methanol is primarily used as an intermediate in the synthesis of agrochemicals and pharmaceuticals. Its structure, featuring a trifluoromethyl group and a chloro substituent, makes it valuable in the development of compounds with enhanced biological activity. In agrochemicals, it is utilized in the production of herbicides and pesticides, where the trifluoromethyl group contributes to improved efficacy and stability. In the pharmaceutical industry, it serves as a building block for the creation of active pharmaceutical ingredients (APIs), particularly in the design of molecules targeting specific enzymes or receptors. Its versatility in chemical reactions allows for the creation of diverse derivatives, expanding its application in drug discovery and crop protection.
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