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CAS 1218790-97-6

:

B-[6-(Phenylmethoxy)-1H-indol-2-yl]boronic acid

Description:
B-[6-(Phenylmethoxy)-1H-indol-2-yl]boronic acid is an organic compound characterized by the presence of a boronic acid functional group, which is known for its ability to form reversible covalent bonds with diols. This compound features an indole structure, which is a bicyclic compound consisting of a benzene ring fused to a pyrrole ring, contributing to its aromatic properties. The phenylmethoxy group enhances its solubility and reactivity, making it useful in various chemical reactions, particularly in Suzuki coupling reactions, which are pivotal in organic synthesis for forming carbon-carbon bonds. The boronic acid moiety also plays a significant role in medicinal chemistry, as it can interact with biological targets, potentially influencing enzyme activity. Additionally, the compound's structural features suggest potential applications in materials science and pharmaceuticals, particularly in the development of targeted therapies or as intermediates in the synthesis of more complex molecules. Overall, B-[6-(Phenylmethoxy)-1H-indol-2-yl]boronic acid exemplifies the versatility of boronic acids in both synthetic and biological contexts.
Formula:C15H14BNO3
InChI:InChI=1S/C15H14BNO3/c18-16(19)15-8-12-6-7-13(9-14(12)17-15)20-10-11-4-2-1-3-5-11/h1-9,17-19H,10H2
InChI key:InChIKey=NPFJJCROCCUTSJ-UHFFFAOYSA-N
SMILES:B(O)(O)C=1NC=2C(C1)=CC=C(OCC3=CC=CC=C3)C2
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