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CAS 2121511-41-7

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B-(2,5-Dichloro-3-fluorophenyl)boronic acid

Description:
B-(2,5-Dichloro-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 two chlorine atoms and one fluorine atom. This compound typically exhibits properties common to boronic acids, such as the ability to form reversible complexes with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. The presence of halogen substituents can influence its reactivity, solubility, and biological activity. Generally, boronic acids are known for their role in Suzuki coupling reactions, which are pivotal in the formation of carbon-carbon bonds in organic synthesis. Additionally, the specific substitutions on the phenyl ring can affect the compound's electronic properties and steric hindrance, potentially impacting its interactions in biological systems. Overall, B-(2,5-Dichloro-3-fluorophenyl)boronic acid is a versatile compound with significant implications in both synthetic and pharmaceutical chemistry.
Formula:C6H4BCl2FO2
InChI:InChI=1S/C6H4BCl2FO2/c8-3-1-4(7(11)12)6(9)5(10)2-3/h1-2,11-12H
InChI key:InChIKey=VLKZUOKRWNZSPW-UHFFFAOYSA-N
SMILES:B(O)(O)C1=C(Cl)C(F)=CC(Cl)=C1
Synonyms:
  • B-(2,5-Dichloro-3-fluorophenyl)boronic acid
  • Boronic acid, B-(2,5-dichloro-3-fluorophenyl)-
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