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Catalog Number:
07320
CAS Number:
269078-77-5
Acide Fmoc-( R , S -3-amino-3-(1-naphtyl)propionique
Purity:
≥ 98 % (HPLC)
Synonym(s):
Fmoc-DL-β-Ala-(1-naphtyl)-OH
Documents
$106.96 /250 mg
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Product Information

Fmoc-(R,S)-3-amino-3-(1-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 valuable in the design of bioactive peptides. Researchers and industry professionals can leverage this compound in the development of novel therapeutics, especially in the fields of oncology and neurology, where peptide-based drugs are gaining traction.

The compound's stability and ease of handling make it an ideal choice for solid-phase peptide synthesis (SPPS), allowing for efficient and high-yield production of complex peptides. Additionally, its ability to facilitate the introduction of naphthyl residues can lead to improved binding affinities and biological activities of the resulting peptides. With its proven track record in peptide chemistry, Fmoc-(R,S)-3-amino-3-(1-naphthyl)propionic acid stands out as a key reagent for researchers aiming to innovate in drug discovery and development.

Synonyms
Fmoc-DL-β-Ala-(1-naphtyl)-OH
CAS Number
269078-77-5
Purity
≥ 98 % (HPLC)
Molecular Formula
C 28 H 234
Molecular Weight
437.5
MDL Number
MFCD02090642
PubChem ID
2756161
Appearance
Poudre blanche
Conditions
Conserver à 0-8 °C
General Information
Synonyms
Fmoc-DL-β-Ala-(1-naphtyl)-OH
CAS Number
269078-77-5
Purity
≥ 98 % (HPLC)
Molecular Formula
C 28 H 234
Molecular Weight
437.5
MDL Number
MFCD02090642
PubChem ID
2756161
Appearance
Poudre blanche
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,S)-3-amino-3-(1-naphthyl)propionic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protecting group for amino acids in solid-phase peptide synthesis, allowing for the selective addition of amino acids while preventing unwanted reactions.
  • Drug Development: Its unique structure can enhance the bioactivity of peptide-based drugs, making it valuable in pharmaceutical research aimed at developing new therapeutics.
  • Bioconjugation: The compound is used in bioconjugation processes, linking peptides to other molecules, such as fluorescent tags or drug carriers, to improve targeting and efficacy in drug delivery systems.
  • Research in Neuroscience: Due to its naphthyl group, it can be utilized in studies related to neuropeptides, potentially aiding in the understanding of neurological pathways and disorders.
  • Material Science: Its properties can be exploited in the development of novel materials, such as hydrogels, which can be used in tissue engineering and regenerative medicine.

Citations