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Catalog Number:
04943
CAS Number:
204322-11-2
Fmoc-3-amino-1-carboxymethyl-pyridin-2-one
Purity:
≥ 97% (HPLC)
Synonym(s):
Fmoc-Acpo-OH
Documents
$194.99 /250MG
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Product Information

Fmoc-3-amino-1-carboxymethyl-pyridin-2-one is a versatile compound 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 the synthesis of peptides. Its unique structure allows for efficient coupling reactions, making it an ideal choice for researchers focusing on the development of complex peptide sequences. The carboxymethyl group enhances its solubility in various solvents, facilitating its use in diverse chemical environments.

In addition to its role in peptide synthesis, Fmoc-3-amino-1-carboxymethyl-pyridin-2-one has potential applications in medicinal chemistry, particularly in the design of bioactive compounds. Its ability to act as a building block in the synthesis of pyridine derivatives opens avenues for the development of novel pharmaceuticals. Researchers can leverage its properties to create targeted therapies, enhancing the efficacy of drug candidates. With its robust performance and adaptability, this compound stands out as a valuable asset in both academic and industrial laboratories.

Synonyms
Fmoc-Acpo-OH
CAS Number
204322-11-2
Purity
≥ 97% (HPLC)
Molecular Formula
C22H18N2O5
Molecular Weight
390.41
MDL Number
MFCD00673785
PubChem ID
2756138
Appearance
Off-white powder
Conditions
Store at 0-8 °C
General Information
Synonyms
Fmoc-Acpo-OH
CAS Number
204322-11-2
Purity
≥ 97% (HPLC)
Molecular Formula
C22H18N2O5
Molecular Weight
390.41
MDL Number
MFCD00673785
PubChem ID
2756138
Appearance
Off-white powder
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-amino-1-carboxymethyl-pyridin-2-one is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protecting group in the synthesis of peptides, allowing for selective reactions without interference from other functional groups.
  • Drug Development: It plays a crucial role in the development of pharmaceutical compounds, particularly in designing drugs that target specific biological pathways.
  • Bioconjugation: The chemical is used in bioconjugation processes, enabling the attachment of biomolecules to surfaces or other molecules, which is essential in creating targeted therapies.
  • Analytical Chemistry: It is utilized in analytical methods to enhance the detection and quantification of various compounds, improving the accuracy of results in research laboratories.
  • Material Science: The compound finds applications in the development of advanced materials, particularly in creating polymers with specific functional properties for various industrial applications.

Citations