Pinacol 2-Chloro-6 - (trifluoromethyl) pyridine-4-borate
95%
- Product Code: 42965
CAS:
1218790-05-6
| Molecular Weight: | 307.50 g./mol | Molecular Formula: | C₁₂H₁₄BClF₃NO₂ |
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| EC Number: | MDL Number: | MFCD13195760 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8℃, dry, airtight |
Product Description:
Pinacol 2-Chloro-6-(trifluoromethyl) pyridine-4-borate is primarily utilized in organic synthesis as a versatile building block for the creation of complex molecules. Its borate ester functionality makes it a valuable reagent in cross-coupling reactions, particularly Suzuki-Miyaura coupling, which is widely employed in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. The trifluoromethyl and chloro substituents on the pyridine ring enhance its reactivity and provide opportunities for further functionalization, making it useful in the development of compounds with specific electronic or steric properties. Additionally, its stability and compatibility with various reaction conditions make it a preferred choice in medicinal chemistry for designing drug candidates and bioactive molecules.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | Ft68,167.78 |
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| 1.000 | 10-20 days | Ft130,517.54 |
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| 5.000 | 10-20 days | Ft339,384.40 |
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Pinacol 2-Chloro-6 - (trifluoromethyl) pyridine-4-borate
Pinacol 2-Chloro-6-(trifluoromethyl) pyridine-4-borate is primarily utilized in organic synthesis as a versatile building block for the creation of complex molecules. Its borate ester functionality makes it a valuable reagent in cross-coupling reactions, particularly Suzuki-Miyaura coupling, which is widely employed in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. The trifluoromethyl and chloro substituents on the pyridine ring enhance its reactivity and provide opportunities for further functionalization, making it useful in the development of compounds with specific electronic or steric properties. Additionally, its stability and compatibility with various reaction conditions make it a preferred choice in medicinal chemistry for designing drug candidates and bioactive molecules.
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