5-Cyclopentyl-6-trifluoromethylpyridine-3-boronic acid
95%
- Product Code: 58781
CAS:
2225171-85-5
| Molecular Weight: | 259.0326296 g./mol | Molecular Formula: | C₁₁H₁₃BF₃NO₂ |
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| Density: | Storage Condition: | -20℃, sealed and dry |
Product Description:
5-Cyclopentyl-6-trifluoromethylpyridine-3-boronic acid is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. This reaction is widely employed in the pharmaceutical industry for the construction of complex molecules, including active pharmaceutical ingredients (APIs). The boronic acid group in this compound acts as a key functional group, enabling the formation of carbon-carbon bonds with aryl or vinyl halides in the presence of a palladium catalyst. Its cyclopentyl and trifluoromethyl substituents contribute to the steric and electronic properties, making it a valuable building block for designing molecules with specific biological activities. Additionally, it finds applications in material science for the development of organic electronic materials and advanced polymers. Its stability and reactivity make it a versatile reagent in both academic research and industrial processes.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.005 | 10-20 days | ฿10,520.00 |
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| 0.025 | 10-20 days | ฿45,060.00 |
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| 0.100 | 10-20 days | ฿135,200.00 |
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5-Cyclopentyl-6-trifluoromethylpyridine-3-boronic acid
5-Cyclopentyl-6-trifluoromethylpyridine-3-boronic acid is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. This reaction is widely employed in the pharmaceutical industry for the construction of complex molecules, including active pharmaceutical ingredients (APIs). The boronic acid group in this compound acts as a key functional group, enabling the formation of carbon-carbon bonds with aryl or vinyl halides in the presence of a palladium catalyst. Its cyclopentyl and trifluoromethyl substituents contribute to the steric and electronic properties, making it a valuable building block for designing molecules with specific biological activities. Additionally, it finds applications in material science for the development of organic electronic materials and advanced polymers. Its stability and reactivity make it a versatile reagent in both academic research and industrial processes.
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