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Catalog Number:
15673
CAS Number:
501015-35-6
Fmoc-(S-3-amino-3-(2,3-dichlorophenyl)propionic acid
Synonym(s):
Fmoc-L-β-Phe(2,3-DiCl)-OH, (S-Fmoc-2,3-dichloro-β-phenylalanine
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Product Information

Fmoc-(S)-3-amino-3-(2,3-dichlorophenyl)propionic acid is a versatile building block widely utilized in peptide synthesis and medicinal chemistry. This compound features a unique structure that includes a fluorenylmethoxycarbonyl (Fmoc) protecting group, which is essential for the selective protection of amino groups during the synthesis of peptides. Its specific stereochemistry and the presence of the dichlorophenyl moiety enhance its reactivity and compatibility with various coupling reagents, making it an ideal choice for researchers focused on developing novel peptides with tailored properties.

In addition to its applications in peptide synthesis, this compound is also relevant in the development of pharmaceuticals, particularly in the design of inhibitors and modulators for various biological targets. Its unique properties allow for the exploration of structure-activity relationships, facilitating the discovery of new therapeutic agents. Researchers in the fields of drug discovery and development will find Fmoc-(S)-3-amino-3-(2,3-dichlorophenyl)propionic acid to be an invaluable tool in their quest for innovative solutions in healthcare.

Synonyms
Fmoc-L-β-Phe(2,3-DiCl)-OH, (S-Fmoc-2,3-dichloro-β-phenylalanine
CAS Number
501015-35-6
Molecular Formula
C24H19Cl2NO4
Molecular Weight
456.32
MDL Number
MFCD03427981
PubChem ID
2759188
Conditions
Store at 0-8°C
General Information
Synonyms
Fmoc-L-β-Phe(2,3-DiCl)-OH, (S-Fmoc-2,3-dichloro-β-phenylalanine
CAS Number
501015-35-6
Molecular Formula
C24H19Cl2NO4
Molecular Weight
456.32
MDL Number
MFCD03427981
PubChem ID
2759188
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-(2,3-dichlorophenyl)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 (SPPS), allowing for the creation of complex peptide sequences with high purity and yield.
  • Drug Development: Its unique structure makes it valuable in the pharmaceutical industry for developing new drugs, especially those targeting specific receptors, enhancing the efficacy and selectivity of therapeutic agents.
  • Bioconjugation: The compound can be used in bioconjugation processes, where it helps attach biomolecules to surfaces or other molecules, facilitating the development of targeted drug delivery systems.
  • Research in Neuroscience: It plays a role in studying neurotransmitter systems, particularly in the design of compounds that can modulate synaptic activity, which is crucial for understanding various neurological disorders.
  • Analytical Chemistry: This chemical is employed in analytical methods for detecting and quantifying amino acids and peptides, providing researchers with reliable data for their studies.

Citations