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CAS 1256359-09-7

:

1-Methyl-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indazole

Description:
1-Methyl-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indazole is a chemical compound characterized by its unique structure, which includes an indazole core substituted with a methyl group and a dioxaborolane moiety. The presence of the dioxaborolane group suggests potential applications in organoboron chemistry, particularly in cross-coupling reactions, which are valuable in synthetic organic chemistry. The compound's indazole structure contributes to its potential biological activity, as indazoles are known for their diverse pharmacological properties. Additionally, the presence of multiple methyl groups in the dioxaborolane enhances its steric bulk, which can influence reactivity and solubility. This compound may exhibit interesting properties such as fluorescence or specific interactions with biological targets, making it a candidate for further research in medicinal chemistry and materials science. Its CAS number, 1256359-09-7, allows for precise identification and retrieval of information in chemical databases. Overall, this compound represents a fusion of organic and boron chemistry with potential applications in various fields.
Formula:C14H19BN2O2
InChI:InChI=1S/C14H19BN2O2/c1-13(2)14(3,4)19-15(18-13)11-7-6-10-9-16-17(5)12(10)8-11/h6-9H,1-5H3
InChI key:InChIKey=SHPRKJZVUGXCTM-UHFFFAOYSA-N
SMILES:CC1(C)OB(C=2C=C3C(=CC2)C=NN3C)OC1(C)C
Synonyms:
  • 1-Methyl-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indazole
  • 1H-Indazole, 1-methyl-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-
  • 1-Methyl-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)indazole
  • 1-methyl-6-(tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indazole
  • 1-Methyl-1H-indazol-6-ylboronic acid pinacol ester
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