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CAS 58237-94-8

:

[(tert-butoxycarbonyl)amino](1H-indol-3-yl)acetic acid

Description:
[(tert-butoxycarbonyl)amino](1H-indol-3-yl)acetic acid, with the CAS number 58237-94-8, is a chemical compound that features a distinctive structure combining an indole moiety with an amino acid derivative. This compound is characterized by the presence of a tert-butoxycarbonyl (Boc) protecting group, which is commonly used in organic synthesis to protect amines during chemical reactions. The indole ring contributes to the compound's potential biological activity, as indole derivatives are often found in various natural products and pharmaceuticals. The acetic acid component provides acidic properties, which can influence solubility and reactivity. This compound is typically utilized in peptide synthesis and medicinal chemistry, where the Boc group can be selectively removed to reveal the free amine for further functionalization. Its stability under standard laboratory conditions makes it a valuable intermediate in synthetic pathways. Overall, the unique combination of functional groups in this compound allows for diverse applications in chemical research and drug development.
Formula:C15H18N2O4
InChI:InChI=1/C15H18N2O4/c1-15(2,3)21-14(20)17-12(13(18)19)10-8-16-11-7-5-4-6-9(10)11/h4-8,12,16H,1-3H3,(H,17,20)(H,18,19)
SMILES:CC(C)(C)OC(=NC(c1c[nH]c2ccccc12)C(=O)O)O
Synonyms:
  • 1H-Indole-3-acetic acid, alpha-[[(1,1-dimethylethoxy)carbonyl]amino]-
  • N-Boc-(3-Indole)glycine
  • [(tert-Butoxycarbonyl)amino](1H-indol-3-yl)acetic acid
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