(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
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.
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Size (g) Availability Price Quantity
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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