(4-fluoro-3-(4-oxopiperidine-1-carbonyl)phenyl)boronic acid
98%
- Product Code: 89288
CAS:
1704082-33-6
Molecular Weight: | 265.05 g./mol | Molecular Formula: | C₁₂H₁₃BFNO₄ |
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EC Number: | MDL Number: | MFCD28400453 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its boronic acid group enables the formation of carbon-carbon bonds, making it valuable in the production of pharmaceuticals and complex organic molecules. The fluorine substituent enhances its reactivity and selectivity, allowing for precise modifications in drug development. Additionally, the presence of the piperidine carbonyl group contributes to its potential use in creating bioactive compounds, particularly those targeting neurological and metabolic disorders. Its structural features make it a versatile intermediate in medicinal chemistry and material science.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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1.000 | 10-20 days | £1,135.15 |
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(4-fluoro-3-(4-oxopiperidine-1-carbonyl)phenyl)boronic acid
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its boronic acid group enables the formation of carbon-carbon bonds, making it valuable in the production of pharmaceuticals and complex organic molecules. The fluorine substituent enhances its reactivity and selectivity, allowing for precise modifications in drug development. Additionally, the presence of the piperidine carbonyl group contributes to its potential use in creating bioactive compounds, particularly those targeting neurological and metabolic disorders. Its structural features make it a versatile intermediate in medicinal chemistry and material science.
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