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Catalog Number:
31952
CAS Number:
204716-07-4
Fmoc-4-acetil-L-fenilalanina
Purity:
≥ 99,5 % (HPLC quiral)
Synonym(s):
Fmoc-L-Phe(4-Ac)-OH, Fmoc- p -acetil-Phe-OH, Fmoc-Phe(4-Ac)-OH
Documents
$130.00 /100 mg
Tamaño
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Product Information

Fmoc-4-acetyl-L-phenylalanine 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 amino groups during solid-phase peptide synthesis. Its unique structure, characterized by the acetyl group on the phenylalanine side chain, enhances the compound's stability and solubility, making it an ideal choice for researchers looking to optimize peptide sequences.

In practical applications, Fmoc-4-acetyl-L-phenylalanine is particularly valuable in the synthesis of bioactive peptides and pharmaceuticals, where precise control over the amino acid sequence is crucial. Its ability to facilitate the incorporation of modified amino acids into peptides allows for the development of novel therapeutic agents with improved efficacy and specificity. Researchers in the fields of medicinal chemistry and biochemistry will find this compound indispensable for advancing their projects, particularly in the design of peptide-based drugs and biomolecules.

Synonyms
Fmoc-L-Phe(4-Ac)-OH, Fmoc- p -acetil-Phe-OH, Fmoc-Phe(4-Ac)-OH
CAS Number
204716-07-4
Purity
≥ 99,5 % (HPLC quiral)
Molecular Formula
C26H23NO5
Molecular Weight
429.46
MDL Number
MFCD01317022
PubChem ID
21908899
Appearance
Polvo de color blanco a blanquecino
Optical Rotation
[a] D 20 = - 7 ± 2 ° (C=1 en MeOH)
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
Fmoc-L-Phe(4-Ac)-OH, Fmoc- p -acetil-Phe-OH, Fmoc-Phe(4-Ac)-OH
CAS Number
204716-07-4
Purity
≥ 99,5 % (HPLC quiral)
Molecular Formula
C26H23NO5
Molecular Weight
429.46
MDL Number
MFCD01317022
PubChem ID
21908899
Appearance
Polvo de color blanco a blanquecino
Optical Rotation
[a] D 20 = - 7 ± 2 ° (C=1 en MeOH)
Conditions
Conservar entre 0 y 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-4-acetyl-L-phenylalanine 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.
  • Drug Development: Its unique structure aids in the design of peptide-based pharmaceuticals, providing researchers with a versatile tool for developing new therapeutic agents targeting various diseases.
  • Bioconjugation: Fmoc-4-acetyl-L-phenylalanine can be used in bioconjugation techniques, facilitating the attachment of peptides to other biomolecules, enhancing the efficacy of drug delivery systems.
  • Research in Protein Engineering: This compound is valuable in the modification of proteins, allowing scientists to explore structure-function relationships and improve protein stability and activity.
  • Fluorescent Labeling: Its properties enable the incorporation of fluorescent tags in peptides, which is crucial for tracking and visualizing biological processes in live cells.

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