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CAS 913835-68-4

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{1-[tert-butyl(dimethyl)silyl]-1H-indol-5-yl}boronic acid

Description:
{1-[tert-butyl(dimethyl)silyl]-1H-indol-5-yl}boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group, which is known for its reactivity in various organic transformations, particularly in Suzuki coupling reactions. The compound features an indole moiety, which contributes to its aromatic properties and potential biological activity. The tert-butyl(dimethyl)silyl group enhances the compound's stability and solubility, making it suitable for various synthetic applications. This compound is typically used in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals, due to its ability to form covalent bonds with other organic molecules. Additionally, boronic acids are known for their ability to form reversible complexes with diols, which can be exploited in sensor technology and drug delivery systems. Overall, the unique structural features of this compound make it a valuable intermediate in synthetic chemistry.
Formula:C14H22BNO2Si
InChI:InChI=1/C14H22BNO2Si/c1-14(2,3)19(4,5)16-9-8-11-10-12(15(17)18)6-7-13(11)16/h6-10,17-18H,1-5H3
SMILES:CC(C)(C)[Si](C)(C)n1ccc2cc(ccc12)B(O)O
Synonyms:
  • (1-(tert-Butyldimethylsilyl)-1H-indol-5-yl)boronicacid
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