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CAS 1150271-44-5

:

1,3-Dihydro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2H-indol-2-one

Description:
1,3-Dihydro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2H-indol-2-one is a chemical compound characterized by its unique structure, which includes an indole core fused with a dioxaborolane moiety. This compound features a bicyclic indole structure, which is known for its biological activity and potential pharmaceutical applications. The presence of the dioxaborolane group enhances its reactivity and solubility, making it useful in various synthetic applications, particularly in organic synthesis and medicinal chemistry. The tetramethyl substituents contribute to its steric bulk, influencing its interactions with other molecules. Additionally, the compound may exhibit interesting electronic properties due to the conjugated system within the indole structure. Its specific applications and reactivity can be further explored in the context of drug development and material science, where boron-containing compounds are often utilized for their unique properties. Overall, this compound represents a fascinating intersection of organic chemistry and potential therapeutic utility.
Formula:C14H18BNO3
InChI:InChI=1S/C14H18BNO3/c1-13(2)14(3,4)19-15(18-13)10-6-5-7-11-9(10)8-12(17)16-11/h5-7H,8H2,1-4H3,(H,16,17)
InChI key:InChIKey=LDDMKYKRLRAKPL-UHFFFAOYSA-N
SMILES:O=C1CC2=C(C=CC=C2N1)B3OC(C)(C)C(C)(C)O3
Synonyms:
  • 1,3-Dihydro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2H-indol-2-one
  • 4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)indolin-2-one
  • 2H-Indol-2-one, 1,3-dihydro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-
  • Oxindole-4-boronic acid pinacal ester
  • Oxindole-4-boronic acid picol ester
  • (2-OXOINDOLIN-4-YL)BORONIC ACID PINACOL ESTER
  • Oxindole-4-boronic acid pinacol ester
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