🌟 99% Happy customers

📦 Same-day shipping on in-stock items

Catalog Number:
15715
CAS Number:
507472-11-9
Fmoc-(S-3-amino-3-(2-naphthyl)propionic acid
Purity:
≥ 99% (HPLC)
Synonym(s):
Fmoc-L-β-Ala-(2-naphthyl)-OH
Documents
$72.31 /100MG
Pack Size Availability Price
Request Bulk Quote
Product Information

Fmoc-(S)-3-amino-3-(2-naphthyl)propionic acid is a versatile building block widely utilized in peptide synthesis and medicinal chemistry. This compound features a fluorenylmethoxycarbonyl (Fmoc) protective group, which is essential for the selective protection of amino acids during solid-phase peptide synthesis. Its unique structure, incorporating a naphthyl group, enhances the compound's hydrophobicity, making it particularly valuable in the development of peptide-based therapeutics and research applications. Researchers appreciate its ability to facilitate the synthesis of complex peptides, enabling the exploration of novel drug candidates with improved efficacy and specificity.

In addition to its role in peptide synthesis, Fmoc-(S)-3-amino-3-(2-naphthyl)propionic acid has shown potential in the development of biomaterials and drug delivery systems. Its compatibility with various coupling reagents and its stability under standard reaction conditions make it an ideal choice for chemists looking to streamline their synthetic processes. With its robust performance and adaptability, this compound stands out as a key player in advancing peptide chemistry and related fields.

Synonyms
Fmoc-L-β-Ala-(2-naphthyl)-OH
CAS Number
507472-11-9
Purity
≥ 99% (HPLC)
Molecular Formula
C28H23NO4
Molecular Weight
437.49
MDL Number
MFCD03427991
PubChem ID
2756164
Melting Point
189-194 ºC
Appearance
White powder
Optical Rotation
[a]D25 = -38 ± 2º (C=1 in DMF)
Conditions
Store at 0-8 °C
General Information
Synonyms
Fmoc-L-β-Ala-(2-naphthyl)-OH
CAS Number
507472-11-9
Purity
≥ 99% (HPLC)
Molecular Formula
C28H23NO4
Molecular Weight
437.49
MDL Number
MFCD03427991
PubChem ID
2756164
Melting Point
189-194 ºC
Appearance
White powder
Optical Rotation
[a]D25 = -38 ± 2º (C=1 in DMF)
Conditions
Store at 0-8 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

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

  • Peptide Synthesis: This compound serves as a protecting group for amino acids in peptide synthesis, allowing for the selective modification of amino acids without affecting the overall structure.
  • Drug Development: Its unique structure can be incorporated into drug candidates, particularly in the design of biologically active peptides, enhancing their stability and bioavailability.
  • Bioconjugation: The compound can be used in bioconjugation processes, facilitating the attachment of biomolecules to surfaces or other molecules, which is crucial in developing targeted therapies.
  • Material Science: In polymer chemistry, it can be utilized to create functionalized polymers, which can be applied in various fields such as drug delivery systems and biosensors.
  • Research in Neuroscience: Its structural properties make it a valuable tool in studying neuropeptides, contributing to the understanding of neurological functions and potential treatments for related disorders.

Citations