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CAS 1451393-44-4

:

B-(4-Chloro-2-fluoro-3-formylphenyl)boronic acid

Description:
B-(4-Chloro-2-fluoro-3-formylphenyl)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 a chloro and a fluoro group, as well as an aldehyde (formyl) group. This compound typically exhibits properties such as being a solid at room temperature, with potential solubility in polar organic solvents due to the presence of the boronic acid moiety. The boronic acid group is known for its 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 the compound's reactivity and electronic properties, potentially enhancing its utility in cross-coupling reactions or as a building block in the synthesis of more complex molecules. Additionally, the compound may exhibit interesting biological activities, making it a candidate for further research in pharmaceutical applications.
Formula:C7H5BClFO3
InChI:InChI=1S/C7H5BClFO3/c9-6-2-1-5(8(12)13)7(10)4(6)3-11/h1-3,12-13H
InChI key:InChIKey=AMEOCAKEWZXMRO-UHFFFAOYSA-N
SMILES:C(=O)C1=C(F)C(B(O)O)=CC=C1Cl
Synonyms:
  • B-(4-Chloro-2-fluoro-3-formylphenyl)boronic acid
  • Boronic acid, B-(4-chloro-2-fluoro-3-formylphenyl)-
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