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CAS 870777-33-6

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B-(3-Formyl-5-methylphenyl)boronic acid

Description:
B-(3-Formyl-5-methylphenyl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group and an aldehyde moiety. This compound features a phenyl ring substituted with a formyl group at the 3-position and a methyl group at the 5-position, contributing to its unique reactivity and potential applications in organic synthesis. The boronic acid functionality allows for participation in various reactions, such as Suzuki coupling, making it valuable in the formation of carbon-carbon bonds. Additionally, the presence of the formyl group provides opportunities for further functionalization, enabling the synthesis of more complex molecules. This compound is typically a solid at room temperature and may exhibit solubility in polar organic solvents. Its reactivity and functional groups make it of interest in medicinal chemistry and materials science, particularly in the development of pharmaceuticals and advanced materials. As with many boronic acids, care should be taken in handling due to potential reactivity with moisture and air, which can lead to hydrolysis.
Formula:C8H9BO3
InChI:InChI=1S/C8H9BO3/c1-6-2-7(5-10)4-8(3-6)9(11)12/h2-5,11-12H,1H3
InChI key:InChIKey=IDXLUNCVVBZUEN-UHFFFAOYSA-N
SMILES:B(O)(O)C1=CC(C=O)=CC(C)=C1
Synonyms:
  • B-(3-Formyl-5-methylphenyl)boronic acid
  • (3-Formyl-5-methylphenyl)boronic acid
  • Boronic acid, (3-formyl-5-methylphenyl)-
  • Boronic acid, B-(3-formyl-5-methylphenyl)-
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