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Catalog Number:
14472
CAS Number:
1076196-99-0
Fmoc-3-amino-6-methyl-1-carboxymethyl-pyridin-2-one
Purity:
≥ 98% (HPLC)
Documents
$79.22 /25MG
Pack Size Availability Price
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Product Information

Fmoc-3-amino-6-methyl-1-carboxymethyl-pyridin-2-one is a versatile compound widely utilized in the field of peptide synthesis and drug development. This compound features a unique Fmoc (9-fluorenylmethoxycarbonyl) protecting group, which is essential for the selective protection of amines during the synthesis of peptides. Its structure allows for efficient coupling reactions, making it an ideal choice for researchers focused on developing complex peptide sequences. The presence of the carboxymethyl and methyl groups enhances its solubility and reactivity, facilitating smoother synthesis processes and improving yields.

In addition to its role in peptide synthesis, Fmoc-3-amino-6-methyl-1-carboxymethyl-pyridin-2-one has potential applications in medicinal chemistry, particularly in the design of novel therapeutic agents. Its unique structural features may contribute to the development of compounds with improved bioactivity and specificity. Researchers in pharmaceutical and biochemistry fields will find this compound invaluable for its ability to streamline synthesis and enhance the efficacy of peptide-based drugs.

CAS Number
1076196-99-0
Purity
≥ 98% (HPLC)
Molecular Formula
C23H20N2O5
Molecular Weight
404.2
MDL Number
MFCD04974228
Melting Point
215-224 °C
Appearance
White powder
Conditions
Store at 0-8 °C
General Information
CAS Number
1076196-99-0
Purity
≥ 98% (HPLC)
Molecular Formula
C23H20N2O5
Molecular Weight
404.2
MDL Number
MFCD04974228
Melting Point
215-224 °C
Appearance
White powder
Conditions
Store at 0-8 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Fmoc-3-amino-6-methyl-1-carboxymethyl-pyridin-2-one is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, allowing for the introduction of specific amino acid sequences that are essential in drug development and biological research.
  • Drug Discovery: Its unique structure enables researchers to explore new therapeutic agents, particularly in the fields of oncology and neurology, where targeted therapies are increasingly important.
  • Bioconjugation: The compound is useful in bioconjugation processes, facilitating the attachment of biomolecules to surfaces or other molecules, which is crucial in creating effective drug delivery systems.
  • Fluorescent Probes: It can be modified to create fluorescent probes for imaging applications, helping scientists visualize cellular processes in real-time, which is vital in cellular biology and pharmacology.
  • Research in Catalysis: The compound's properties make it a candidate for catalysis research, potentially leading to more efficient chemical reactions in various industrial applications.

Citations