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CAS 58438-04-3

:

(S)-N-BOC-2-Naphthylalanine

Description:
(S)-N-BOC-2-Naphthylalanine, with the CAS number 58438-04-3, is an amino acid derivative characterized by the presence of a naphthyl group and a tert-butyloxycarbonyl (BOC) protecting group on the amino functionality. This compound is typically used in peptide synthesis and as a building block in organic chemistry due to its ability to form stable peptide bonds. The BOC group serves as a protective moiety that can be removed under acidic conditions, allowing for selective functionalization of the amino group. The naphthyl moiety contributes to the compound's hydrophobic characteristics, influencing its solubility and interaction with biological systems. Additionally, the stereochemistry indicated by the (S) designation suggests that this compound has a specific spatial arrangement, which can significantly affect its biological activity and interactions. Overall, (S)-N-BOC-2-Naphthylalanine is valued in research and pharmaceutical applications for its structural properties and versatility in synthetic chemistry.
Formula:C18H21NO4
InChI:InChI=1/C18H21NO4/c1-18(2,3)23-17(22)19-15(16(20)21)11-12-8-9-13-6-4-5-7-14(13)10-12/h4-10,15H,11H2,1-3H3,(H,19,22)(H,20,21)/t15-/m0/s1
SMILES:CC(C)(C)OC(=N[C@@H](Cc1ccc2ccccc2c1)C(=O)O)O
Synonyms:
  • Boc-L-2-Naphthylalanine
  • N-tert-Butoxycarbonyl-2-naphthyl-L-alanine
  • Boc-2-Nal-OH
  • Boc-Ala(2-Naphthyl)-OH
  • NALPHA-tert-Butoxycarbonyl-3-(2-naphthyl)-L-alanine
  • Boc-L-3-(2-Naphthyl)alanine
  • N-(tert-butoxycarbonyl)-3-naphthalen-2-yl-D-alanine
  • (2S)-2-[(tert-butoxycarbonyl)amino]-3-naphthalen-2-ylpropanoate
  • N-(tert-butoxycarbonyl)-3-naphthalen-2-yl-L-alanine
  • Boc-3-(2-Naphthyl)-L-alanine
  • BOC-3-(2-naphthyl)-2-alanine
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