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Catalog Number:
15600
CAS Number:
507472-24-4
Fmoc-(S-3-amino-3-(4-cyanophenyl)propionic acid
Purity:
≥ 99% (HPLC)
Synonym(s):
Fmoc-L-β-Phe(4-CN)-OH, (S-Fmoc-4-cyano-β-phenylalanine
Documents
$65.00 /100MG
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Product Information

Fmoc-(S)-3-amino-3-(4-cyanophenyl)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 allows for selective deprotection during the synthesis process, making it an essential tool for chemists working on complex peptide sequences. Its structural characteristics, including the presence of a cyanophenyl group, enhance its utility in creating peptides with specific biological activities, particularly in the fields of medicinal chemistry and biochemistry.

Researchers and industry professionals can leverage Fmoc-(S)-3-amino-3-(4-cyanophenyl)propionic acid for the development of novel therapeutics, especially in the design of peptide-based drugs targeting various diseases. Its ability to facilitate the introduction of functional groups while maintaining stability under standard reaction conditions makes it a preferred choice for high-throughput screening and combinatorial chemistry applications. This compound not only streamlines the synthesis process but also improves the overall yield and purity of the final products, making it a valuable asset in any chemical laboratory.

Synonyms
Fmoc-L-β-Phe(4-CN)-OH, (S-Fmoc-4-cyano-β-phenylalanine
CAS Number
507472-24-4
Purity
≥ 99% (HPLC)
Molecular Formula
C25H20N2O4
Molecular Weight
412.44
MDL Number
MFCD03428006
PubChem ID
2759184
Melting Point
106-112 °C
Appearance
White solid
Optical Rotation
[a]D25 = -35 ± 2º (C=1 in DMF)
Conditions
Store at 0-8 °C
General Information
Synonyms
Fmoc-L-β-Phe(4-CN)-OH, (S-Fmoc-4-cyano-β-phenylalanine
CAS Number
507472-24-4
Purity
≥ 99% (HPLC)
Molecular Formula
C25H20N2O4
Molecular Weight
412.44
MDL Number
MFCD03428006
PubChem ID
2759184
Melting Point
106-112 °C
Appearance
White solid
Optical Rotation
[a]D25 = -35 ± 2º (C=1 in DMF)
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-(4-cyanophenyl)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 structures with high purity.
  • Drug Development: It plays a significant role in pharmaceutical research, where it is used to develop new drug candidates, particularly in the field of neuropharmacology, due to its ability to modify peptide properties.
  • Bioconjugation: The compound is useful in bioconjugation processes, enabling researchers to attach biomolecules to surfaces or other molecules, which is vital in creating targeted drug delivery systems.
  • Fluorescent Probes: Its unique structure allows it to be utilized in the development of fluorescent probes for imaging applications, enhancing the visualization of biological processes in live cells.
  • Research on Protein Interactions: This chemical aids in studying protein-protein interactions, providing insights into cellular mechanisms and potential therapeutic targets in various diseases.

Citations