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Catalog Number:
15666
CAS Number:
511272-37-0
Acide Fmoc-( R -3-amino-3-(2,4-dichlorophényl)propionique
Synonym(s):
Fmoc-D-β-Phe(2,4-DiCl)-OH, ( R -Fmoc-2,4-Dichloro-β-phénylalanine
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Product Information

Fmoc-(R)-3-amino-3-(2,4-dichlorophenyl)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 complex peptides. Its unique structure, characterized by the presence of a 2,4-dichlorophenyl group, enhances its reactivity and allows for the development of novel bioactive compounds. Researchers and industry professionals appreciate its role in the design of peptide-based therapeutics, particularly in the fields of drug discovery and development.

This compound is particularly valuable in the synthesis of peptides with specific biological activities, enabling the exploration of new therapeutic avenues. Its stability and compatibility with various coupling reagents make it an ideal choice for solid-phase peptide synthesis (SPPS). Additionally, the presence of the dichlorophenyl moiety may impart unique pharmacological properties, making it a candidate for further investigation in pharmaceutical applications. With its robust profile, Fmoc-(R)-3-amino-3-(2,4-dichlorophenyl)propionic acid stands out as a key building block in the advancement of peptide chemistry.

Synonyms
Fmoc-D-β-Phe(2,4-DiCl)-OH, ( R -Fmoc-2,4-Dichloro-β-phénylalanine
CAS Number
511272-37-0
Molecular Formula
C 24 H 19 Cl 2 NO 4
Molecular Weight
456.32
MDL Number
MFCD03428018
PubChem ID
22309348
Conditions
Conserver à 0-8°C
General Information
Synonyms
Fmoc-D-β-Phe(2,4-DiCl)-OH, ( R -Fmoc-2,4-Dichloro-β-phénylalanine
CAS Number
511272-37-0
Molecular Formula
C 24 H 19 Cl 2 NO 4
Molecular Weight
456.32
MDL Number
MFCD03428018
PubChem ID
22309348
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-(2,4-dichlorophenyl)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 without interfering with other functional groups.
  • Drug Development: Its unique structure makes it valuable in the design of novel pharmaceuticals, particularly in creating compounds that target specific biological pathways.
  • Bioconjugation: Researchers use it to attach biomolecules to surfaces or other molecules, enhancing the functionality of drugs and diagnostics in biomedicine.
  • Research in Neuroscience: The compound's ability to interact with neurotransmitter systems makes it a candidate for studying neurological disorders and developing potential treatments.
  • Material Science: It can be incorporated into polymer matrices, improving the mechanical properties and thermal stability of materials used in various industrial applications.

Citations