3-Acetyl-2-fluorophenylboronic acid

98%

  • Product Code: 44750
  CAS:    870778-95-3
Molecular Weight: 181.96 g./mol Molecular Formula: C₈H₈BFO₃
EC Number: MDL Number:
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Density: Storage Condition: 2-8℃
Product Description: 3-Acetyl-2-fluorophenylboronic acid is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. This reaction is widely employed in the pharmaceutical industry for the construction of carbon-carbon bonds, enabling the synthesis of complex molecules, including drug candidates. The acetyl and fluorine substituents on the phenyl ring can influence the reactivity and selectivity of the boronic acid, making it valuable for designing specific molecular architectures. Additionally, it may serve as an intermediate in the development of bioactive compounds, including enzyme inhibitors or receptor modulators, due to its unique structural features. Its application extends to material science, where it can be used to modify surfaces or create functionalized polymers with tailored properties.
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
100.000 10-20 days $1,902.16
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3-Acetyl-2-fluorophenylboronic acid
3-Acetyl-2-fluorophenylboronic acid is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. This reaction is widely employed in the pharmaceutical industry for the construction of carbon-carbon bonds, enabling the synthesis of complex molecules, including drug candidates. The acetyl and fluorine substituents on the phenyl ring can influence the reactivity and selectivity of the boronic acid, making it valuable for designing specific molecular architectures. Additionally, it may serve as an intermediate in the development of bioactive compounds, including enzyme inhibitors or receptor modulators, due to its unique structural features. Its application extends to material science, where it can be used to modify surfaces or create functionalized polymers with tailored properties.
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