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Catalog Number:
15447
CAS Number:
479064-92-1
Fmoc-(R-3-amino-3-(4-chlorophenyl)propionic acid
Synonym(s):
Fmoc-D-β-Phe(4-Cl)-OH, (R-Fmoc-4-chloro-β-phenylalanine
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Product Information

Fmoc-(R)-3-amino-3-(4-chlorophenyl)propionic acid is a versatile building block widely utilized in peptide synthesis and drug development. This compound features a unique Fmoc (9-fluorenylmethoxycarbonyl) protecting group, which facilitates the selective protection of amino groups during the synthesis of peptides. Its structural characteristics, including the presence of a 4-chlorophenyl group, enhance its reactivity and compatibility with various coupling reagents, making it an ideal choice for researchers in the fields of medicinal chemistry and biochemistry.

In practical applications, Fmoc-(R)-3-amino-3-(4-chlorophenyl)propionic acid has been employed in the design of bioactive peptides and pharmaceuticals, contributing to advancements in targeted therapies and drug delivery systems. Its ability to provide stability and solubility in aqueous environments further supports its use in complex biological systems. Researchers appreciate its efficiency in streamlining peptide synthesis, allowing for the rapid development of novel compounds with therapeutic potential.

Synonyms
Fmoc-D-β-Phe(4-Cl)-OH, (R-Fmoc-4-chloro-β-phenylalanine
CAS Number
479064-92-1
Molecular Formula
C24H20ClNO4
Molecular Weight
421.88
MDL Number
MFCD03428036
PubChem ID
2764209
Conditions
Store at 0-8°C
General Information
Synonyms
Fmoc-D-β-Phe(4-Cl)-OH, (R-Fmoc-4-chloro-β-phenylalanine
CAS Number
479064-92-1
Molecular Formula
C24H20ClNO4
Molecular Weight
421.88
MDL Number
MFCD03428036
PubChem ID
2764209
Conditions
Store at 0-8°C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Fmoc-(R)-3-amino-3-(4-chlorophenyl)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, allowing for the creation of complex peptide structures with high purity.
  • Drug Development: It is used in the development of pharmaceutical compounds, especially in creating bioactive peptides that can serve as potential therapeutic agents in various medical applications.
  • Bioconjugation: The chemical is valuable in bioconjugation processes, where it helps attach peptides to other molecules, enhancing the efficacy and targeting of drug delivery systems.
  • Research in Neuroscience: Its derivatives are explored in neuroscience research for their potential roles in modulating neurotransmitter systems, contributing to the understanding of neurological disorders.
  • Material Science: The compound is also investigated for its applications in creating functional materials, such as hydrogels, which can be used in drug delivery and tissue engineering.

Citations