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Catalog Number:
15599
CAS Number:
517905-92-9
Fmoc-(R-3-amino-3-(4-cyanophenyl)propionic acid
Synonym(s):
Fmoc-D-β-Phe(4-CN)-OH, (R-Fmoc-4-cyano-β-phenylalanine
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Product Information

Fmoc-(R)-3-amino-3-(4-cyanophenyl)propionic acid is a versatile building block widely utilized in peptide synthesis and medicinal chemistry. This compound features a unique Fmoc (9-fluorenylmethoxycarbonyl) protecting group, which facilitates the selective deprotection of amino acids during the synthesis process. Its structural characteristics, including the presence of a cyanophenyl group, enhance its reactivity and compatibility with various coupling reactions, making it an excellent choice for researchers focused on developing novel peptides and bioactive compounds.

In the pharmaceutical industry, Fmoc-(R)-3-amino-3-(4-cyanophenyl)propionic acid is particularly valuable for the design of peptide-based therapeutics, including those targeting specific receptors or enzymes. Its ability to improve solubility and stability in biological systems further underscores its relevance in drug formulation. Researchers can leverage this compound to create tailored peptides with enhanced efficacy and specificity, paving the way for innovative solutions in drug discovery and development.

Synonyms
Fmoc-D-β-Phe(4-CN)-OH, (R-Fmoc-4-cyano-β-phenylalanine
CAS Number
517905-92-9
Molecular Formula
C25H20N2O4
Molecular Weight
412.44
MDL Number
MFCD03428044
PubChem ID
2759184
Conditions
Store at 0-8°C
General Information
Synonyms
Fmoc-D-β-Phe(4-CN)-OH, (R-Fmoc-4-cyano-β-phenylalanine
CAS Number
517905-92-9
Molecular Formula
C25H20N2O4
Molecular Weight
412.44
MDL Number
MFCD03428044
PubChem ID
2759184
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-cyanophenyl)propionic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in solid-phase peptide synthesis, allowing researchers to create complex peptides with specific sequences and functionalities.
  • Drug Development: Its unique structure aids in the design of novel pharmaceuticals, particularly in developing compounds that target specific biological pathways, enhancing therapeutic efficacy.
  • Bioconjugation: The chemical is valuable in bioconjugation techniques, where it can be used to attach biomolecules to surfaces or other molecules, improving drug delivery systems.
  • Research in Neuroscience: Its application in studying neurotransmitter systems and receptor interactions provides insights into neurological disorders, making it a crucial tool for researchers in this field.
  • Fluorescent Probes: The compound can be modified to create fluorescent probes for imaging applications, enabling real-time observation of cellular processes in biological research.