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CAS 229639-48-9

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(3S)-3-[(tert-butoxycarbonyl)amino]-4-(1H-indol-3-yl)butanoic acid

Description:
The chemical substance known as (3S)-3-[(tert-butoxycarbonyl)amino]-4-(1H-indol-3-yl)butanoic acid, with the CAS number 229639-48-9, is an amino acid derivative characterized by the presence of an indole moiety and a tert-butoxycarbonyl (Boc) protecting group on the amino function. This compound features a chiral center at the 3-position, contributing to its stereochemistry. The indole group is known for its aromatic properties and biological significance, often found in various natural products and pharmaceuticals. The tert-butoxycarbonyl group serves as a protective group for the amino group, facilitating synthetic processes by preventing unwanted reactions. This compound is likely to exhibit solubility in organic solvents and may have limited solubility in water, typical of many amino acid derivatives with hydrophobic components. Its structural features suggest potential applications in medicinal chemistry, particularly in the design of bioactive compounds or as intermediates in peptide synthesis. Overall, this compound exemplifies the complexity and versatility of amino acid derivatives in chemical research and development.
Formula:C17H22N2O4
InChI:InChI=1/C17H22N2O4/c1-17(2,3)23-16(22)19-12(9-15(20)21)8-11-10-18-14-7-5-4-6-13(11)14/h4-7,10,12,18H,8-9H2,1-3H3,(H,19,22)(H,20,21)/t12-/m0/s1
SMILES:CC(C)(C)OC(=N[C@@H](Cc1c[nH]c2ccccc12)CC(=O)O)O
Synonyms:
  • Boc-β-HoTrp-OH
  • Boc-L-Beta-Homotryptophan
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