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CAS 1072812-23-7

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7-Bromo-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole

Description:
7-Bromo-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole is a chemical compound characterized by its indole core, which is a bicyclic structure containing a benzene ring fused to a pyrrole ring. The presence of a bromine atom at the 7-position enhances its reactivity and potential applications in organic synthesis and medicinal chemistry. The compound also features a boron-containing moiety, specifically a dioxaborolane, which is known for its utility in various chemical reactions, including Suzuki coupling reactions. The tetramethyl substitution on the dioxaborolane contributes to the compound's stability and steric hindrance, influencing its reactivity and solubility. This compound may be of interest in the development of pharmaceuticals or agrochemicals due to the unique properties imparted by both the indole and boron functionalities. Its specific applications would depend on further studies regarding its biological activity and reactivity in synthetic pathways.
Formula:C14H17BBrNO2
InChI:InChI=1S/C14H17BBrNO2/c1-13(2)14(3,4)19-15(18-13)11-8-9-6-5-7-10(16)12(9)17-11/h5-8,17H,1-4H3
InChI key:InChIKey=KGWJGQUTNNLURY-UHFFFAOYSA-N
SMILES:CC1(C)OB(OC1(C)C)C=2NC=3C(C2)=CC=CC3Br
Synonyms:
  • 7-Bromo-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole
  • 1H-Indole, 7-bromo-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-
  • 7-Bromoindole-2-boronic acid pinacol ester
  • 7-BROMO-1H-INDOLE-2-BORONIC ACID PINACOL ESTER
  • 7-Bromo-1H-indole-2-boronic acid picol ester
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