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CAS 871329-52-1

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(2-Chloro-3-fluorophenyl)boronic acid

Description:
(2-Chloro-3-fluorophenyl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a phenyl ring that is substituted with both chlorine and fluorine atoms. This compound typically exhibits a white to off-white crystalline solid form and is soluble in polar solvents such as water and alcohols, owing to the boronic acid group. The presence of the chlorine and fluorine substituents can influence its reactivity and interactions, making it useful in various chemical applications, particularly in organic synthesis and medicinal chemistry. Boronic acids are known for their ability to form reversible covalent bonds with diols, which is a key feature in applications such as drug development and materials science. Additionally, (2-Chloro-3-fluorophenyl)boronic acid may serve as a building block in the synthesis of more complex molecules, including pharmaceuticals and agrochemicals, due to its functional versatility. Safety data should be consulted for handling and storage, as with all chemical substances.
Formula:C6H5BClFO2
InChI:InChI=1S/C6H5BClFO2/c8-6-4(7(10)11)2-1-3-5(6)9/h1-3,10-11H
InChI key:InChIKey=TYOGIUGNZOBBHE-UHFFFAOYSA-N
SMILES:B(O)(O)C1=C(Cl)C(F)=CC=C1
Synonyms:
  • (2-Chloro-3-fluorophenyl)boronic acid
  • B-(2-Chloro-3-fluorophenyl)boronic acid
  • Boronic Acid, B-(2-Chloro-3-Fluorophenyl)-
  • Boronic acid, (2-chloro-3-fluorophenyl)-
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