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CAS 850568-62-6

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[5-(benzyloxy)-1-(tert-butoxycarbonyl)-1H-indol-2-yl]boronic acid

Description:
[5-(Benzyloxy)-1-(tert-butoxycarbonyl)-1H-indol-2-yl]boronic acid is a boronic acid derivative characterized by the presence of an indole ring, which is a bicyclic structure composed of a benzene fused to a pyrrole. This compound features a benzyloxy group and a tert-butoxycarbonyl (Boc) protecting group, which are commonly used in organic synthesis to enhance solubility and stability. The boronic acid functional group is known for its ability to form reversible covalent bonds with diols, making it valuable in various applications, including Suzuki coupling reactions in organic synthesis. The presence of the Boc group suggests that the compound may be used in peptide synthesis or as a precursor for further functionalization. Additionally, the compound's structure indicates potential biological activity, as indole derivatives are often found in pharmaceuticals. Overall, this compound exemplifies the intersection of organic chemistry and medicinal chemistry, showcasing the utility of boronic acids in synthetic methodologies.
Formula:C20H22BNO5
InChI:InChI=1/C20H22BNO5/c1-20(2,3)27-19(23)22-17-10-9-16(11-15(17)12-18(22)21(24)25)26-13-14-7-5-4-6-8-14/h4-12,24-25H,13H2,1-3H3
SMILES:CC(C)(C)OC(=O)n1c2ccc(cc2cc1B(O)O)OCc1ccccc1
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