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Catalog Number:
15709
CAS Number:
507472-10-8
Fmoc-(S)-3-amino-3-(1-naphthyl)propionic acid
Purity:
≥ 99% (HPLC)
Synonym(s):
Fmoc-L-β-Ala-(1-naphthyl)-OH
Documents
$80.30 /250MG
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Product Information

Fmoc-(S)-3-amino-3-(1-naphthyl)propionic acid is a versatile building block widely utilized in peptide synthesis and medicinal chemistry. This compound features a fluorenylmethoxycarbonyl (Fmoc) protecting group, which is essential for the selective protection of amino groups during the synthesis of peptides. Its unique structure, characterized by the presence of a naphthyl group, enhances the compound's hydrophobic interactions, making it particularly valuable in the development of bioactive peptides and pharmaceuticals. Researchers and industry professionals appreciate its ability to facilitate the formation of complex peptide sequences while maintaining stability under various reaction conditions.

In addition to its role in peptide synthesis, Fmoc-(S)-3-amino-3-(1-naphthyl)propionic acid has shown promise in the development of novel therapeutic agents, particularly in the fields of cancer research and drug delivery systems. Its specific stereochemistry contributes to the compound's effectiveness in biological applications, allowing for the design of targeted therapies. With its favorable properties and practical applications, this compound stands out as an essential tool for researchers aiming to innovate in peptide-based drug development.

Synonyms
Fmoc-L-β-Ala-(1-naphthyl)-OH
CAS Number
507472-10-8
Purity
≥ 99% (HPLC)
Molecular Formula
C28H23NO4
Molecular Weight
437.49
MDL Number
MFCD03427990
PubChem ID
2756161
Melting Point
202 - 208 °C (Lit.)
Appearance
White to off-white powder
Optical Rotation
[a]D20 = 31 ± 2 º (C=1 in DMF)
Conditions
Store at 0 - 8 °C
General Information
Synonyms
Fmoc-L-β-Ala-(1-naphthyl)-OH
CAS Number
507472-10-8
Purity
≥ 99% (HPLC)
Molecular Formula
C28H23NO4
Molecular Weight
437.49
MDL Number
MFCD03427990
PubChem ID
2756161
Melting Point
202 - 208 °C (Lit.)
Appearance
White to off-white powder
Optical Rotation
[a]D20 = 31 ± 2 º (C=1 in DMF)
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

Fmoc-(S)-3-amino-3-(1-naphthyl)propionic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in solid-phase peptide synthesis, allowing researchers to create complex peptides with high purity and yield.
  • Drug Development: Its unique structure aids in designing novel pharmaceuticals, particularly in the development of drugs targeting specific receptors, enhancing therapeutic efficacy.
  • Bioconjugation: The Fmoc group facilitates the attachment of biomolecules, making it valuable in creating bioconjugates for targeted drug delivery systems in cancer therapy.
  • Research in Neuroscience: This compound is used in studies related to neurotransmitter function, helping to explore the role of amino acids in brain signaling pathways.
  • Material Science: It is applied in the development of functional materials, such as sensors and nanomaterials, due to its ability to form stable interactions with various substrates.

Citations