2-Chloro-3-fluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine
95%
- Product Code: 42840
CAS:
1416367-16-2
| Molecular Weight: | 257.4968 g./mol | Molecular Formula: | C₁₁H₁₄BClFNO₂ |
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| EC Number: | MDL Number: | MFCD07787387 | |
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| Density: | Storage Condition: | room temperature |
Product Description:
This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction, where it acts as a key intermediate for constructing complex molecules. Its boronate ester group enables efficient coupling with aryl or vinyl halides, making it valuable in the development of pharmaceuticals, agrochemicals, and advanced materials. Additionally, its pyridine ring structure contributes to its use in designing bioactive compounds, including potential drug candidates targeting various diseases. The fluorine and chlorine substituents further enhance its reactivity and selectivity in synthetic pathways, making it a versatile tool in medicinal chemistry and material science research.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | $107.36 |
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2-Chloro-3-fluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine
This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction, where it acts as a key intermediate for constructing complex molecules. Its boronate ester group enables efficient coupling with aryl or vinyl halides, making it valuable in the development of pharmaceuticals, agrochemicals, and advanced materials. Additionally, its pyridine ring structure contributes to its use in designing bioactive compounds, including potential drug candidates targeting various diseases. The fluorine and chlorine substituents further enhance its reactivity and selectivity in synthetic pathways, making it a versatile tool in medicinal chemistry and material science research.
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