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CAS 957034-29-6

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[4-bromo-1-(tert-butoxycarbonyl)-1H-indol-2-yl]boronic acid

Description:
[4-bromo-1-(tert-butoxycarbonyl)-1H-indol-2-yl]boronic acid is a boronic acid derivative characterized by the presence of a bromine atom and a tert-butoxycarbonyl (Boc) protecting group on an indole structure. This compound typically exhibits properties associated with both boronic acids and indole derivatives, such as moderate solubility in organic solvents and potential reactivity in cross-coupling reactions, which are valuable in organic synthesis and medicinal chemistry. The boronic acid functional group allows for the formation of covalent bonds with diols and other nucleophiles, making it useful in various applications, including drug development and materials science. The presence of the Boc group provides a means to protect the amine functionality during synthetic procedures, which can be deprotected under mild acidic conditions. Overall, this compound is of interest in the field of organic chemistry for its versatility and reactivity, particularly in the synthesis of complex organic molecules.
Formula:C13H15BBrNO4
InChI:InChI=1/C13H15BBrNO4/c1-13(2,3)20-12(17)16-10-6-4-5-9(15)8(10)7-11(16)14(18)19/h4-7,18-19H,1-3H3
SMILES:CC(C)(C)OC(=O)n1c2cccc(c2cc1B(O)O)Br
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