(2-Chloro-5-fluoropyridin-4-yl)boronic acid
98%
- Product Code: 89786
CAS:
951677-47-7
| Molecular Weight: | 175.35 g./mol | Molecular Formula: | C₅H₄BClFNO₂ |
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| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | 334.4°C | |
| Density: | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate for the construction of complex molecules, especially in the pharmaceutical and agrochemical industries. Its boronic acid group enables it to form carbon-carbon bonds with aryl or vinyl halides, facilitating the production of biaryl compounds. These biaryl structures are often found in active pharmaceutical ingredients (APIs) and agrochemicals, making it valuable for drug discovery and crop protection research. Additionally, its pyridine ring with chloro and fluoro substituents enhances its reactivity and selectivity in coupling reactions, making it a versatile building block for synthesizing heterocyclic compounds.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.250 | 10-20 days | ฿1,476.00 |
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| 1.000 | 10-20 days | ฿3,717.00 |
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| 5.000 | 10-20 days | ฿11,178.00 |
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(2-Chloro-5-fluoropyridin-4-yl)boronic acid
This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate for the construction of complex molecules, especially in the pharmaceutical and agrochemical industries. Its boronic acid group enables it to form carbon-carbon bonds with aryl or vinyl halides, facilitating the production of biaryl compounds. These biaryl structures are often found in active pharmaceutical ingredients (APIs) and agrochemicals, making it valuable for drug discovery and crop protection research. Additionally, its pyridine ring with chloro and fluoro substituents enhances its reactivity and selectivity in coupling reactions, making it a versatile building block for synthesizing heterocyclic compounds.
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