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Catalog Number:
15714
CAS Number:
511272-48-3
Acide Fmoc-( R )-3-amino-3-(2-naphtyl)propionique
Purity:
≥ 98 % (HPLC)
Synonym(s):
Fmoc-D-β-Ala-(2-naphtyl)-OH
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$70.00 /100 mg
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Product Information

Fmoc-(R)-3-amino-3-(2-naphthyl)propionic acid is a versatile building block widely utilized in peptide synthesis and drug development. 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 useful in the development of bioactive peptides and pharmaceuticals. Researchers in the fields of medicinal chemistry and biochemistry can leverage this compound for the synthesis of complex peptide sequences, facilitating the exploration of new therapeutic agents.

The compound's stability and ease of use in solid-phase peptide synthesis (SPPS) provide significant advantages over similar compounds, allowing for higher yields and purities in peptide production. Its application extends to the development of peptide-based drugs, where the naphthyl moiety can contribute to improved binding affinities and biological activities. With its robust profile, Fmoc-(R)-3-amino-3-(2-naphthyl)propionic acid is an essential tool for researchers aiming to innovate in peptide chemistry and drug formulation.

Synonyms
Fmoc-D-β-Ala-(2-naphtyl)-OH
CAS Number
511272-48-3
Purity
≥ 98 % (HPLC)
Molecular Formula
C 28 H 234
Molecular Weight
437.49
MDL Number
MFCD03428029
PubChem ID
2756164
Melting Point
187 - 193 ?C
Appearance
Solide blanc
Optical Rotation
[a] D 25 = +38 ± 2 º (C = 1 dans DMF)
Conditions
Conserver à 0 - 8 °C
General Information
Synonyms
Fmoc-D-β-Ala-(2-naphtyl)-OH
CAS Number
511272-48-3
Purity
≥ 98 % (HPLC)
Molecular Formula
C 28 H 234
Molecular Weight
437.49
MDL Number
MFCD03428029
PubChem ID
2756164
Melting Point
187 - 193 ?C
Appearance
Solide blanc
Optical Rotation
[a] D 25 = +38 ± 2 º (C = 1 dans DMF)
Conditions
Conserver à 0 - 8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

Fmoc-(R)-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 structures with high purity.
  • Drug Development: Its unique structural properties make it valuable in the pharmaceutical industry for designing novel drug candidates, especially those targeting specific biological pathways.
  • Bioconjugation: The compound can be used to create bioconjugates, linking biomolecules to drugs or imaging agents, enhancing their efficacy and specificity in therapeutic applications.
  • Research in Neuroscience: It plays a role in studying neuropeptides and their functions, contributing to the understanding of neurological disorders and potential treatments.
  • Material Science: This chemical is also explored in the development of functional materials, particularly in creating polymers with specific properties for use in various industrial applications.

Citations