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CAS 1000068-23-4

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1-(tert-butoxycarbonyl)-4-methoxy-1H-indol-2-ylboronic acid

Description:
1-(tert-Butoxycarbonyl)-4-methoxy-1H-indol-2-ylboronic acid is a boronic acid derivative characterized by the presence of a boron atom bonded to an indole structure, which is a bicyclic compound consisting of a benzene ring fused to a pyrrole ring. This compound features a tert-butoxycarbonyl (Boc) protecting group, which is commonly used in organic synthesis to protect amines during reactions. The methoxy group attached to the indole ring enhances its solubility and reactivity. As a boronic acid, it can participate in Suzuki coupling reactions, making it valuable in the synthesis of complex organic molecules, particularly in pharmaceutical chemistry. The presence of both the boronic acid and the indole moiety suggests potential applications in medicinal chemistry, particularly in the development of compounds with biological activity. Additionally, the compound's stability and reactivity can be influenced by factors such as pH and the presence of other functional groups, making it a versatile building block in organic synthesis.
Formula:C14H18BNO5
InChI:InChI=1S/C14H18BNO5/c1-14(2,3)21-13(17)16-10-6-5-7-11(20-4)9(10)8-12(16)15(18)19/h5-8,18-19H,1-4H3
SMILES:CC(C)(C)OC(=O)n1c2cccc(c2cc1B(O)O)OC
Synonyms:
  • 1H-indole-1-carboxylic acid, 2-borono-4-methoxy-, 1,1-dimethylethyl ester
  • [1-(tert-butoxycarbonyl)-4-methoxy-1H-indol-2-yl]boronic acid
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