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Catalog Number:
29680
CAS Number:
454424-73-8
Acide R , S -Fmoc-3-amino-2-(naphtalène-2-ylméthyl)-propionique
Purity:
≥ 97 % (HPLC)
Documents
$134.70 /25 mg
Taille
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Product Information

(R,S)-Fmoc-3-amino-2-(naphthalen-2-ylmethyl)-propionic acid is a versatile compound widely utilized in peptide synthesis and medicinal chemistry. This amino acid derivative features a fluorenylmethoxycarbonyl (Fmoc) protecting group, which is essential for the selective protection of amines during the synthesis of peptides. Its unique structure, incorporating a naphthylmethyl group, enhances the compound's hydrophobicity, making it particularly valuable in the development of bioactive peptides and pharmaceuticals. Researchers appreciate its ability to facilitate the formation of stable peptide bonds while maintaining the integrity of sensitive functional groups.

This compound is especially relevant in the fields of drug discovery and development, where it can be employed to create novel peptide-based therapeutics. Its application extends to the synthesis of peptide libraries for high-throughput screening, allowing scientists to explore a wide array of biological activities. Additionally, (R,S)-Fmoc-3-amino-2-(naphthalen-2-ylmethyl)-propionic acid stands out for its compatibility with various coupling reagents, making it a preferred choice for chemists looking to optimize their synthetic pathways.

CAS Number
454424-73-8
Purity
≥ 97 % (HPLC)
Molecular Formula
C 29 H 254
Molecular Weight
451.52
MDL Number
MFCD11226812
PubChem ID
45356719
Melting Point
163-173 ?C
Appearance
Poudre blanche
Conditions
Conserver à 0-8°C
General Information
CAS Number
454424-73-8
Purity
≥ 97 % (HPLC)
Molecular Formula
C 29 H 254
Molecular Weight
451.52
MDL Number
MFCD11226812
PubChem ID
45356719
Melting Point
163-173 ?C
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

(R,S)-Fmoc-3-amino-2-(naphthalen-2-ylmethyl)-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, enhancing the efficiency and yield of desired peptide sequences.
  • Drug Development: It is used in the design of novel pharmaceuticals, especially in the development of peptide-based drugs, due to its ability to improve stability and bioavailability.
  • Bioconjugation: The compound can be employed in bioconjugation techniques, allowing for the attachment of biomolecules to surfaces or other molecules, which is crucial in creating targeted drug delivery systems.
  • Research in Neuroscience: It plays a role in studying neuroactive peptides, which can help in understanding neurological disorders and developing potential treatments.
  • Material Science: This chemical is also explored in the creation of advanced materials, such as hydrogels, that have applications in drug delivery and tissue engineering.

Citations