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Catalog Number:
15062
CAS Number:
269078-81-1
Fmoc-(R,S-3-amino-3-(2-naphthyl)propionic acid
Purity:
≥ 97% (HPLC)
Synonym(s):
Fmoc-DL-β-Ala-(2-naphthyl)-OH
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Product Information

Fmoc-(R,S)-3-amino-3-(2-naphthyl)propionic acid is a versatile building block widely utilized in peptide synthesis and medicinal chemistry. This compound, known for its protective Fmoc (9-fluorenylmethoxycarbonyl) group, facilitates the efficient assembly of peptides by providing a stable and easily removable protecting group for the amino functionality. Its unique structure, featuring a naphthyl side chain, enhances the hydrophobic interactions, making it particularly valuable in the design of bioactive peptides and pharmaceuticals. Researchers appreciate its role in developing compounds with improved potency and selectivity, especially in the fields of drug discovery and development.

In addition to its applications in peptide synthesis, Fmoc-(R,S)-3-amino-3-(2-naphthyl)propionic acid serves as a critical intermediate in the production of various biologically active molecules. Its ability to enhance the stability and solubility of peptides makes it an attractive choice for formulating therapeutic agents. With its proven track record in both academic and industrial settings, this compound stands out for its reliability and effectiveness in advancing peptide-based research and applications.

Synonyms
Fmoc-DL-β-Ala-(2-naphthyl)-OH
CAS Number
269078-81-1
Purity
≥ 97% (HPLC)
Molecular Formula
C28H23NO4
Molecular Weight
437.49
MDL Number
MFCD01863204
PubChem ID
2756164
Appearance
White powder
Conditions
Store at 0-8 °C
General Information
Synonyms
Fmoc-DL-β-Ala-(2-naphthyl)-OH
CAS Number
269078-81-1
Purity
≥ 97% (HPLC)
Molecular Formula
C28H23NO4
Molecular Weight
437.49
MDL Number
MFCD01863204
PubChem ID
2756164
Appearance
White powder
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-(R,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 solid-phase peptide synthesis (SPPS), allowing for the creation of complex peptide sequences with high purity.
  • Drug Development: It plays a crucial role in the development of peptide-based therapeutics, providing researchers with the ability to design and modify peptides that can target specific biological pathways.
  • Bioconjugation: The compound can be used to create bioconjugates, linking peptides to other molecules such as drugs or imaging agents, enhancing their efficacy and specificity in targeted therapies.
  • Research in Neuroscience: Its structural properties make it valuable in studies related to neuropeptides, aiding in the understanding of neurological functions and potential treatments for neurodegenerative diseases.
  • Material Science: This chemical is also explored in the development of novel materials, particularly in creating functionalized polymers that can be used in drug delivery systems.

Citations