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Catalog Number:
29681
CAS Number:
1310680-37-5
Ácido R , S -Fmoc-3-amino-2-(naftalen-1-il)-propiónico
Purity:
≥ 98 % (HPLC)
Documents
$168.35 /100 mg
Tamaño
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Product Information

(R,S)-Fmoc-3-amino-2-(naphthalen-1-yl)-propionic acid is a versatile compound widely utilized in peptide synthesis and drug development. This amino acid derivative, characterized by its fluorenylmethoxycarbonyl (Fmoc) protecting group, offers enhanced stability and solubility, making it an ideal choice for researchers in the fields of medicinal chemistry and biochemistry. Its unique structure allows for efficient incorporation into peptides, facilitating the study of protein interactions and the development of novel therapeutics.

In addition to its applications in peptide synthesis, (R,S)-Fmoc-3-amino-2-(naphthalen-1-yl)-propionic acid serves as a valuable building block in the design of bioactive compounds. Its naphthalene moiety contributes to increased hydrophobicity, which can enhance the binding affinity of drug candidates. Researchers can leverage this compound to explore new avenues in drug discovery, particularly in targeting complex biological pathways. With its robust profile and practical applications, this compound stands out as a key ingredient for advancing pharmaceutical research.

CAS Number
1310680-37-5
Purity
≥ 98 % (HPLC)
Molecular Formula
C28H23NO4
Molecular Weight
437.49
MDL Number
MFCD18782837
PubChem ID
86810496
Melting Point
182-190 ?C
Appearance
Polvo blanquecino
Conditions
Conservar entre 0 y 8 °C.
General Information
CAS Number
1310680-37-5
Purity
≥ 98 % (HPLC)
Molecular Formula
C28H23NO4
Molecular Weight
437.49
MDL Number
MFCD18782837
PubChem ID
86810496
Melting Point
182-190 ?C
Appearance
Polvo blanquecino
Conditions
Conservar entre 0 y 8 °C.
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

(R,S)-Fmoc-3-amino-2-(naphthalen-1-yl)-propionic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protective group in the synthesis of peptides, allowing for the selective modification of amino acids. Its stability under various conditions makes it a preferred choice for researchers in organic chemistry.
  • Drug Development: The compound's unique structure can be leveraged in the design of novel pharmaceuticals, particularly in targeting specific biological pathways. This application is crucial for medicinal chemists aiming to develop more effective treatments.
  • Bioconjugation: It is used in bioconjugation processes to attach biomolecules to surfaces or other molecules, enhancing the functionality of drugs or diagnostic agents in the biomedical field.
  • Material Science: This chemical can be incorporated into polymer matrices to improve material properties, such as strength and thermal stability, which is beneficial for industries focused on advanced materials.
  • Fluorescent Probes: The naphthalene moiety allows for the development of fluorescent probes used in biological imaging, providing researchers with tools to visualize cellular processes in real-time.

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