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CAS 1256359-86-0

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1,1-Dimethylethyl 6-methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole-1-carboxylate

Description:
1,1-Dimethylethyl 6-methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole-1-carboxylate, with CAS number 1256359-86-0, is a chemical compound characterized by its complex structure, which includes an indole moiety and a boron-containing dioxaborolane group. This compound typically exhibits properties associated with both organic and organoboron chemistry, making it of interest in various synthetic applications, particularly in medicinal chemistry and materials science. The presence of the indole structure suggests potential biological activity, as indoles are known for their role in various natural products and pharmaceuticals. The dioxaborolane group may enhance the compound's reactivity and solubility, facilitating its use in cross-coupling reactions or as a boron source in organic synthesis. Additionally, the tert-butyl and methyl substituents contribute to its steric and electronic properties, potentially influencing its reactivity and interaction with biological targets. Overall, this compound represents a unique combination of functional groups that may offer diverse applications in chemical research and development.
Formula:C20H28BNO4
InChI:InChI=1S/C20H28BNO4/c1-13-9-10-14-15(21-25-19(5,6)20(7,8)26-21)12-22(16(14)11-13)17(23)24-18(2,3)4/h9-12H,1-8H3
InChI key:InChIKey=BUUCDWYNFVFACT-UHFFFAOYSA-N
SMILES:C(OC(C)(C)C)(=O)N1C=C(C=2C1=CC(C)=CC2)B3OC(C)(C)C(C)(C)O3
Synonyms:
  • 1H-Indole-1-carboxylic acid, 6-methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-, 1,1-dimethylethyl ester
  • 1,1-Dimethylethyl 6-methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole-1-carboxylate
  • tert-Butyl 6-Methyl-3-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)-1H-indole-1-carboxylate
  • 1-BOC-6-Methylindole-3-boronic acid, pinacol ester
  • t-Butyl 6-methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole-1-carboxylate
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