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CAS 1256355-01-7

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B-(2-Fluoro-5-phenoxyphenyl)boronic acid

Description:
B-(2-Fluoro-5-phenoxyphenyl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group, which is known for its ability to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. The compound features a phenyl ring substituted with a fluorine atom and a phenoxy group, contributing to its unique electronic properties and potential reactivity. The presence of the fluorine atom can enhance the compound's lipophilicity and influence its biological activity. Boronic acids are often utilized in Suzuki coupling reactions, which are pivotal in the formation of carbon-carbon bonds in the synthesis of complex organic molecules. Additionally, the compound may exhibit interesting properties such as solubility in organic solvents and potential interactions with biological targets, making it a candidate for further research in drug development and materials science. Its specific characteristics, such as melting point, solubility, and reactivity, would typically be determined through experimental studies.
Formula:C12H10BFO3
InChI:InChI=1S/C12H10BFO3/c14-12-7-6-10(8-11(12)13(15)16)17-9-4-2-1-3-5-9/h1-8,15-16H
InChI key:InChIKey=HEOPBVFYBMPJNY-UHFFFAOYSA-N
SMILES:O(C1=CC(B(O)O)=C(F)C=C1)C2=CC=CC=C2
Synonyms:
  • (2-Fluoro-5-phenoxyphenyl)boronic acid
  • B-(2-Fluoro-5-phenoxyphenyl)boronic acid
  • Boronic acid, B-(2-fluoro-5-phenoxyphenyl)-
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