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CAS 1451391-37-9

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B-(3-Chloro-2-formyl-4-methylphenyl)boronic acid

Description:
B-(3-Chloro-2-formyl-4-methylphenyl)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 chloro substituent and an aldehyde group on a phenyl ring, contributing to its reactivity and potential for further functionalization. The presence of the methyl group enhances its lipophilicity, which can influence its biological activity and solubility in organic solvents. This compound is typically utilized in cross-coupling reactions, such as Suzuki-Miyaura coupling, to form carbon-carbon bonds, making it valuable in the synthesis of complex organic molecules. Additionally, its unique structural features may impart specific properties that can be exploited in drug development or material science. As with many boronic acids, it is important to handle this compound with care due to its potential reactivity and the need for proper storage conditions to maintain stability.
Formula:C8H8BClO3
InChI:InChI=1S/C8H8BClO3/c1-5-2-3-7(9(12)13)6(4-11)8(5)10/h2-4,12-13H,1H3
InChI key:InChIKey=TUJZIYSBECJNIR-UHFFFAOYSA-N
SMILES:C(=O)C1=C(B(O)O)C=CC(C)=C1Cl
Synonyms:
  • Boronic acid, B-(3-chloro-2-formyl-4-methylphenyl)-
  • B-(3-Chloro-2-formyl-4-methylphenyl)boronic acid
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