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Catalog Number:
16789
CAS Number:
959573-22-9
Fmoc-L-3-carbamoylphénylalanine
Purity:
≥ 96 % (HPLC)
Synonym(s):
Acide Fmoc-(2 S )-2-amino-3-(3-carbamoylphényl)propanoïque
Documents
$75.41 /100 mg
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Product Information

Fmoc-L-3-carbamoylphenylalanine is a versatile amino acid derivative widely utilized in peptide synthesis and drug development. This compound features a fluorenylmethoxycarbonyl (Fmoc) protecting group, which is essential for the selective protection of the amino group during solid-phase peptide synthesis. Its unique structure, characterized by the incorporation of a carbamoylphenyl group, enhances the compound's stability and solubility, making it an excellent choice for researchers focused on developing complex peptides with improved pharmacological properties.

In the pharmaceutical industry, Fmoc-L-3-carbamoylphenylalanine is particularly valuable for the synthesis of bioactive peptides and peptidomimetics, which can lead to the discovery of novel therapeutics. Its application extends to the development of targeted drug delivery systems and the study of protein interactions, offering researchers a powerful tool for advancing their work in medicinal chemistry and biochemistry. With its favorable properties and practical applications, this compound stands out as a key ingredient for professionals aiming to innovate in peptide research and development.

Synonyms
Acide Fmoc-(2 S )-2-amino-3-(3-carbamoylphényl)propanoïque
CAS Number
959573-22-9
Purity
≥ 96 % (HPLC)
Molecular Formula
C25H22N2O5
Molecular Weight
430.45
MDL Number
MFCD06659144
PubChem ID
53398424
Appearance
Poudre blanche à blanc cassé
Optical Rotation
[a] D 25 = -25 ± 5 ° (C = 1 dans DMF)
Conditions
Conserver à 0 - 8 °C
General Information
Synonyms
Acide Fmoc-(2 S )-2-amino-3-(3-carbamoylphényl)propanoïque
CAS Number
959573-22-9
Purity
≥ 96 % (HPLC)
Molecular Formula
C25H22N2O5
Molecular Weight
430.45
MDL Number
MFCD06659144
PubChem ID
53398424
Appearance
Poudre blanche à blanc cassé
Optical Rotation
[a] D 25 = -25 ± 5 ° (C = 1 dans DMF)
Conditions
Conserver à 0 - 8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

Fmoc-L-3-carbamoylphenylalanine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, enabling researchers to create complex structures for various biological studies.
  • Drug Development: Its unique properties make it valuable in the pharmaceutical industry for developing new drugs, particularly those targeting specific proteins or enzymes.
  • Bioconjugation: It is used in bioconjugation processes, allowing scientists to attach biomolecules to surfaces or other molecules, enhancing the functionality of drugs and diagnostics.
  • Protein Engineering: The compound aids in the design of modified proteins with enhanced stability or activity, which is crucial for therapeutic applications.
  • Research in Cancer Therapeutics: Its application in cancer research helps in the development of targeted therapies, providing potential solutions for more effective treatments.

Citations