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CAS 1310383-74-4

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

Description:
B-(1,6-Dimethyl-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 ring. 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 indazole moiety contributes to its potential biological activity, as indazoles are known for their diverse pharmacological properties. The presence of methyl groups at the 1 and 6 positions of the indazole ring can influence the compound's solubility, stability, and reactivity. Additionally, boronic acids are often utilized in cross-coupling reactions, such as Suzuki-Miyaura coupling, which is significant in the formation of carbon-carbon bonds in organic synthesis. Overall, B-(1,6-Dimethyl-1H-indazol-5-yl)boronic acid represents a versatile building block in chemical research and development.
Formula:C9H11BN2O2
InChI:InChI=1S/C9H11BN2O2/c1-6-3-9-7(5-11-12(9)2)4-8(6)10(13)14/h3-5,13-14H,1-2H3
InChI key:InChIKey=VBZJUAROEJPNAK-UHFFFAOYSA-N
SMILES:CN1C=2C(=CC(B(O)O)=C(C)C2)C=N1
Synonyms:
  • (1,6-Dimethyl-1H-indazol-5-yl)boronic acid
  • B-(1,6-Dimethyl-1H-indazol-5-yl)boronic acid
  • 1,6-Dimethyl-1H-indazole-5-boronic acid
  • (1,6-Dimethylindazol-5-yl)boronic acid
  • Boronic acid, B-(1,6-dimethyl-1H-indazol-5-yl)-
  • 1,6-diMethyl-1H-indazol-5-yl-5-boronic acid
  • 5-Borono-1,6-dimethyl-1H-indazole
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