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CAS 40138-17-8

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B-(2-Formyl-5-methylphenyl)boronic acid

Description:
B-(2-Formyl-5-methylphenyl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a phenyl ring that features both a formyl group and a methyl substituent. This compound typically exhibits properties associated with boronic acids, such as the ability to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. The presence of the formyl group introduces reactivity that can facilitate further chemical transformations, while the methyl group can influence the compound's steric and electronic properties. B-(2-Formyl-5-methylphenyl)boronic acid is often utilized in cross-coupling reactions, particularly in the synthesis of complex organic molecules. Its solubility in polar solvents and stability under certain conditions are also notable characteristics. As with many boronic acids, care should be taken in handling due to potential reactivity and the need for proper storage to maintain its integrity.
Formula:C8H9BO3
InChI:InChI=1S/C8H9BO3/c1-6-2-3-7(5-10)8(4-6)9(11)12/h2-5,11-12H,1H3
InChI key:InChIKey=MMKCZTKFYDEERR-UHFFFAOYSA-N
SMILES:B(O)(O)C1=C(C=O)C=CC(C)=C1
Synonyms:
  • B-(2-Formyl-5-methylphenyl)boronic acid
  • Boronic acid, (2-formyl-5-methylphenyl)-
  • boronic acid, B-(2-formyl-5-methylphenyl)-
  • m-Tolueneboronic acid, 6-formyl-
  • 2-Formyl-5-methylphenylboronic acid
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