(2-Fluoro-4-((4-oxopiperidin-1-yl)methyl)phenyl)boronic acid
98%
- Product Code: 89037
CAS:
1704064-22-1
| Molecular Weight: | 251.07 g./mol | Molecular Formula: | C₁₂H₁₅BFNO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD28805545 | |
| Melting Point: | Boiling Point: | ||
| 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 boronic acid reagent, enabling the formation of carbon-carbon bonds, which is crucial in the development of pharmaceuticals and complex organic molecules. Its structure, featuring a fluoro group and a piperidinone moiety, makes it valuable in designing drug candidates, especially those targeting neurological or metabolic disorders. Additionally, it is employed in materials science for creating advanced polymers and functionalized materials with specific electronic or optical properties. Its versatility in chemical transformations makes it a key intermediate in research and industrial applications.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | $2,468.61 |
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(2-Fluoro-4-((4-oxopiperidin-1-yl)methyl)phenyl)boronic acid
This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a boronic acid reagent, enabling the formation of carbon-carbon bonds, which is crucial in the development of pharmaceuticals and complex organic molecules. Its structure, featuring a fluoro group and a piperidinone moiety, makes it valuable in designing drug candidates, especially those targeting neurological or metabolic disorders. Additionally, it is employed in materials science for creating advanced polymers and functionalized materials with specific electronic or optical properties. Its versatility in chemical transformations makes it a key intermediate in research and industrial applications.
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