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Catalog Number:
15070
CAS Number:
133083-34-8
Ácido Fmoc-( R , S )-2-amino-3-(7-metoxi-4-cumaril)propiónico
Purity:
≥ 99 % (HPLC)
Documents
$208.31 /25 mg
Tamaño
Request Bulk Quote
Product Information

Fmoc-(R,S)-2-amino-3-(7-methoxy-4-coumaryl)propionic acid is a versatile compound widely utilized in peptide synthesis and drug development. This amino acid derivative features a protective Fmoc group, which is essential for the selective deprotection of amines during solid-phase peptide synthesis. Its unique structure, incorporating a coumarin moiety, enhances its utility in fluorescence applications, making it an excellent choice for researchers focused on bioimaging and molecular probes.

The compound's ability to facilitate the synthesis of complex peptides allows for the exploration of novel therapeutic agents, particularly in the fields of oncology and neurology. Its stability and compatibility with various coupling reagents further streamline the synthesis process, providing researchers with a reliable tool for developing new biomolecules. With its distinctive properties, Fmoc-(R,S)-2-amino-3-(7-methoxy-4-coumaryl)propionic acid stands out as an essential component in modern chemical research and pharmaceutical development.

CAS Number
133083-34-8
Purity
≥ 99 % (HPLC)
Molecular Formula
C28H23Nº7
Molecular Weight
485.49
MDL Number
MFCD04112691
PubChem ID
2756174
Melting Point
214 - 220 °C
Appearance
Polvo blanco
Conditions
Conservar entre 0 y 8 °C.
General Information
CAS Number
133083-34-8
Purity
≥ 99 % (HPLC)
Molecular Formula
C28H23Nº7
Molecular Weight
485.49
MDL Number
MFCD04112691
PubChem ID
2756174
Melting Point
214 - 220 °C
Appearance
Polvo blanco
Conditions
Conservar entre 0 y 8 °C.
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Fmoc-(R,S)-2-amino-3-(7-methoxy-4-coumaryl)propionic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protective group in solid-phase peptide synthesis, allowing for the selective modification of amino acids while preventing unwanted reactions.
  • Fluorescent Probes: It is used to create fluorescently labeled peptides, which are essential in studying protein interactions and dynamics in cellular environments.
  • Drug Development: Researchers leverage its unique properties to design novel therapeutic agents, particularly in the field of cancer research, where targeting specific pathways is crucial.
  • Bioconjugation: The compound facilitates the attachment of biomolecules to surfaces or other molecules, enhancing the efficacy of diagnostics and targeted drug delivery systems.
  • Analytical Chemistry: It aids in the development of analytical methods for detecting and quantifying biomolecules, providing valuable insights in both clinical and research settings.

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