CymitQuimica logo

CAS 937366-54-6

:

Indole-3-boronic acid pinacol ester

Description:
Indole-3-boronic acid pinacol ester is an organoboron compound characterized by the presence of both an indole moiety and a boronic acid functional group, which is esterified with pinacol. This compound typically exhibits a white to off-white crystalline appearance and is soluble in organic solvents such as dichloromethane and ethanol. It is known for its utility in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it serves as a versatile building block for the formation of carbon-carbon bonds. The boronic acid functionality allows for the formation of stable complexes with diols, making it useful in various applications, including medicinal chemistry and materials science. Additionally, the indole structure contributes to its biological activity, as indole derivatives are often found in pharmaceuticals and natural products. Safety data should be consulted for handling and storage, as with all chemical substances, to ensure proper laboratory practices.
Formula:C14H18BNO2
InChI:InChI=1S/C14H18BNO2/c1-13(2)14(3,4)18-15(17-13)11-9-16-12-8-6-5-7-10(11)12/h5-9,16H,1-4H3
SMILES:CC1(C)C(C)(C)OB(c2c[nH]c3ccccc23)O1
Synonyms:
  • 3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole
  • Indole-3-boronic acid pinacol ester
  • PINACOL ESTER INDOLE-5-BORONIC ACID
  • 3-Indoleboronic Acid Pinacol Ester
  • 1H-Indole-3-boronic acid, pinacol ester
  • 1H-Indole, 3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 3 products.