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CAS 1245816-09-4

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B-(4-Methyl-1H-indazol-5-yl)boronic acid

Description:
B-(4-Methyl-1H-indazol-5-yl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a substituted indazole moiety. This compound typically exhibits properties such as being a white to off-white solid, with solubility in polar solvents like water and alcohols, which is common for boronic acids due to their ability to form hydrogen bonds. The indazole ring contributes to its aromatic character, potentially influencing its reactivity and interactions in chemical reactions, particularly in Suzuki coupling reactions, where boronic acids are valuable intermediates for forming carbon-carbon bonds. Additionally, the presence of the methyl group on the indazole ring can affect the compound's electronic properties and steric hindrance, which may influence its reactivity and selectivity in various applications, including medicinal chemistry and materials science. Overall, B-(4-Methyl-1H-indazol-5-yl)boronic acid is a versatile compound with significant utility in organic synthesis and pharmaceutical development.
Formula:C8H9BN2O2
InChI:InChI=1S/C8H9BN2O2/c1-5-6-4-10-11-8(6)3-2-7(5)9(12)13/h2-4,12-13H,1H3,(H,10,11)
InChI key:InChIKey=IZIRYCSGUBTOOF-UHFFFAOYSA-N
SMILES:CC1=C2C(=CC=C1B(O)O)NN=C2
Synonyms:
  • (4-Methyl-1H-indazol-5-yl)boronic acid
  • B-(4-Methyl-1H-indazol-5-yl)boronic acid
  • Boronic acid, B-(4-methyl-1H-indazol-5-yl)-
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