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Catalog Number:
15559
CAS Number:
507472-16-4
Fmoc-(S)-3-amino-3-(3-chlorophenyl)propionic acid
Synonym(s):
Fmoc-L-β-Phe(3-Cl)-OH, (S-Fmoc-3-chloro-β-phenylalanine
Documents
$206.60 /1G
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Product Information

Fmoc-(S)-3-amino-3-(3-chlorophenyl)propionic acid is a valuable building block in peptide synthesis, particularly in the development of pharmaceuticals and biologically active compounds. This compound features a fluorenylmethoxycarbonyl (Fmoc) protecting group, which is widely recognized for its stability and ease of removal under mild conditions, making it an ideal choice for researchers focused on solid-phase peptide synthesis. Its unique structure, characterized by the presence of a 3-chlorophenyl group, enhances its utility in the design of peptides with specific biological activities, including those targeting receptors or enzymes in various therapeutic areas.

Researchers and industry professionals can leverage Fmoc-(S)-3-amino-3-(3-chlorophenyl)propionic acid in the synthesis of complex peptides, facilitating the exploration of new drug candidates. Its favorable properties allow for efficient coupling reactions, leading to higher yields and purities in peptide synthesis compared to other amino acid derivatives. This compound is particularly relevant in the fields of medicinal chemistry and biochemistry, where the demand for innovative and effective therapeutic agents continues to grow.

Synonyms
Fmoc-L-β-Phe(3-Cl)-OH, (S-Fmoc-3-chloro-β-phenylalanine
CAS Number
507472-16-4
Molecular Formula
C24H20ClNO4
Molecular Weight
421.88
MDL Number
MFCD03427997
PubChem ID
22831638
Conditions
Store at 0-8°C
General Information
Synonyms
Fmoc-L-β-Phe(3-Cl)-OH, (S-Fmoc-3-chloro-β-phenylalanine
CAS Number
507472-16-4
Molecular Formula
C24H20ClNO4
Molecular Weight
421.88
MDL Number
MFCD03427997
PubChem ID
22831638
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-(S)-3-amino-3-(3-chlorophenyl)propionic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound is a key building block in the synthesis of peptides, particularly in solid-phase peptide synthesis (SPPS), allowing for the creation of complex peptide sequences efficiently.
  • Drug Development: Its unique structure makes it valuable in the pharmaceutical industry for developing new drugs, especially those targeting specific biological pathways or diseases.
  • Bioconjugation: The compound can be used in bioconjugation processes, linking biomolecules to therapeutic agents, enhancing the efficacy of targeted therapies.
  • Research in Neuroscience: It serves as a tool in neuroscience research, particularly in studying receptor interactions and signaling pathways involving amino acids.
  • Custom Synthesis: Researchers can utilize this compound for custom synthesis projects, enabling the design of novel compounds for various applications in medicinal chemistry.

Citations