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Catalog Number:
03756
CAS Number:
268734-27-6
Fmoc-3-(9-anthryl)-L-alanine
Purity:
≥ 98.5% (Chiral HPLC)
Synonym(s):
Fmoc-3-(9-anthryl)-L-alanine, Fmoc-3-Ala(9-anthryl)-OH
Documents
$100.00 /25MG
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Product Information

Fmoc-3-(9-anthryl)-L-alanine is a versatile amino acid derivative widely utilized in peptide synthesis and drug development. This compound features a unique anthracene moiety, which enhances its photophysical properties, making it an excellent candidate for applications in fluorescence studies and as a building block in the synthesis of complex peptides. Its Fmoc (fluorenylmethyloxycarbonyl) protecting group allows for easy incorporation into peptide chains while providing stability during synthesis, thus facilitating the production of high-purity peptides for research and therapeutic applications.

Researchers in the fields of medicinal chemistry and biochemistry can leverage Fmoc-3-(9-anthryl)-L-alanine for the development of novel peptide-based drugs, particularly those targeting specific biological pathways or exhibiting unique optical properties. Its ability to serve as a fluorescent probe opens avenues for innovative applications in bioimaging and diagnostics. With its favorable properties and practical applications, this compound stands out as a valuable tool for professionals aiming to advance their research and product development in peptide chemistry.

Synonyms
Fmoc-3-(9-anthryl)-L-alanine, Fmoc-3-Ala(9-anthryl)-OH
CAS Number
268734-27-6
Purity
≥ 98.5% (Chiral HPLC)
Molecular Formula
C32H25NO4
Molecular Weight
487.55
MDL Number
MFCD00671381
PubChem ID
4225821
Appearance
Light yellow to yellow solid
Optical Rotation
[a]D20 = -33 ± 2 º (C=1 in DMF)
Conditions
Store at 0 - 8 °C
General Information
Synonyms
Fmoc-3-(9-anthryl)-L-alanine, Fmoc-3-Ala(9-anthryl)-OH
CAS Number
268734-27-6
Purity
≥ 98.5% (Chiral HPLC)
Molecular Formula
C32H25NO4
Molecular Weight
487.55
MDL Number
MFCD00671381
PubChem ID
4225821
Appearance
Light yellow to yellow solid
Optical Rotation
[a]D20 = -33 ± 2 º (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-3-(9-anthryl)-L-alanine 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.
  • Fluorescent Probes: Its unique anthracene moiety makes it an excellent candidate for developing fluorescent probes, which are used in biological imaging and detection applications, enhancing the visibility of cellular processes.
  • Drug Development: In medicinal chemistry, it is employed to design and optimize drug candidates, particularly those targeting specific proteins, due to its ability to modify the pharmacokinetic properties of peptides.
  • Bioconjugation: The compound is used in bioconjugation techniques to attach biomolecules to surfaces or other molecules, facilitating the development of biosensors and targeted drug delivery systems.
  • Material Science: Its properties are leveraged in the development of advanced materials, such as organic light-emitting diodes (OLEDs), where it contributes to the light-emitting efficiency and stability of the devices.

Citations