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Catalog Number:
15713
CAS Number:
500770-69-4
Boc-(S-3-amino-3-(2-naphthyl)propionic acid
Purity:
≥ 99% (HPLC)
Synonym(s):
Boc-L-β-Ala-(2-naphthyl)-OH
Documents
$72.31 /250MG
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Product Information

Boc-(S)-3-amino-3-(2-naphthyl)propionic acid is a versatile amino acid derivative widely utilized in the synthesis of peptides and pharmaceutical compounds. This compound features a Boc (tert-butyloxycarbonyl) protecting group, which enhances its stability and solubility, making it an ideal choice for researchers in organic synthesis and medicinal chemistry. Its unique structure, characterized by the presence of a naphthyl group, contributes to its potential in developing bioactive molecules, particularly in the fields of drug discovery and development.

In practical applications, Boc-(S)-3-amino-3-(2-naphthyl)propionic acid serves as a building block for the synthesis of various peptide-based therapeutics, offering researchers a reliable option for creating complex molecular architectures. Its ability to facilitate the introduction of chirality in peptide sequences makes it particularly valuable in the design of enantiomerically pure compounds. This compound stands out for its ease of use and compatibility with standard peptide coupling methods, providing significant advantages over similar amino acid derivatives in terms of efficiency and yield.

Synonyms
Boc-L-β-Ala-(2-naphthyl)-OH
CAS Number
500770-69-4
Purity
≥ 99% (HPLC)
Molecular Formula
C18H21NO4
Molecular Weight
315.37
MDL Number
MFCD03427915
PubChem ID
2755990
Appearance
White solid
Optical Rotation
[a]20D = -77.1 ± 3 ° (C=1 in MeOH)
Conditions
Store at 0 - 8 °C
General Information
Synonyms
Boc-L-β-Ala-(2-naphthyl)-OH
CAS Number
500770-69-4
Purity
≥ 99% (HPLC)
Molecular Formula
C18H21NO4
Molecular Weight
315.37
MDL Number
MFCD03427915
PubChem ID
2755990
Appearance
White solid
Optical Rotation
[a]20D = -77.1 ± 3 ° (C=1 in MeOH)
Conditions
Store at 0 - 8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Boc-(S)-3-amino-3-(2-naphthyl)propionic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, particularly in creating modified peptides that can enhance biological activity or stability.
  • Drug Development: It is used in the pharmaceutical industry for developing new drugs, especially those targeting neurological disorders, due to its ability to cross the blood-brain barrier.
  • Bioconjugation: The compound is valuable in bioconjugation processes, where it can be attached to biomolecules to improve their therapeutic properties or targeting capabilities.
  • Research in Neuroscience: It is employed in neuroscience research to study receptor interactions and signaling pathways, helping to uncover mechanisms of action for various neurological drugs.
  • Analytical Chemistry: The compound is used in analytical methods to detect and quantify amino acids and peptides, providing essential data for biochemical research.

Citations