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CAS 1310405-35-6

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B-(6-Methyl-1H-indazol-5-yl)boronic acid

Description:
B-(6-Methyl-1H-indazol-5-yl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a 6-methyl-1H-indazole moiety. This compound typically exhibits properties such as being a white to off-white solid, soluble in polar organic solvents, and possessing a moderate melting point. The boronic acid group 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 indazole structure contributes to its potential biological activity, as indazole derivatives have been studied for their pharmacological properties. Additionally, this compound may participate in Suzuki-Miyaura cross-coupling reactions, which are valuable in the formation of carbon-carbon bonds in organic synthesis. Its unique structural features and reactivity make it a compound of interest in both research and industrial applications, particularly in the development of new materials and pharmaceuticals.
Formula:C8H9BN2O2
InChI:InChI=1S/C8H9BN2O2/c1-5-2-8-6(4-10-11-8)3-7(5)9(12)13/h2-4,12-13H,1H3,(H,10,11)
InChI key:InChIKey=AVTBPALNUPBIAS-UHFFFAOYSA-N
SMILES:B(O)(O)C=1C=C2C(=CC1C)NN=C2
Synonyms:
  • Boronic acid, B-(6-methyl-1H-indazol-5-yl)-
  • B-(6-Methyl-1H-indazol-5-yl)boronic acid
  • (6-Methyl-1H-indazol-5-yl)boronic acid
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