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Catalog Number:
14464
CAS Number:
882847-09-8
Boc-3-amino-1-carboxymethyl-pyridin-2-one
Purity:
≥ 99% (HPLC)
Synonym(s):
Boc-Acpo-OH
Documents
$113.87 /25MG
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Product Information

Boc-3-amino-1-carboxymethyl-pyridin-2-one is a versatile compound widely utilized in pharmaceutical and biochemical research. This compound features a Boc (tert-butyloxycarbonyl) protecting group, which enhances its stability and solubility, making it an ideal candidate for peptide synthesis and drug development. Its unique structure allows for the modification of amino acids, facilitating the design of novel therapeutic agents. Researchers have leveraged this compound in the synthesis of bioactive molecules, particularly in the development of inhibitors for various biological targets.

The practical applications of Boc-3-amino-1-carboxymethyl-pyridin-2-one extend to medicinal chemistry, where it serves as a building block for complex organic molecules. Its ability to form stable intermediates is crucial in the synthesis of compounds with potential anti-cancer and anti-inflammatory properties. Additionally, its compatibility with various reaction conditions makes it a preferred choice for chemists looking to streamline their synthetic pathways. With its promising applications and unique properties, this compound stands out as a valuable tool for researchers aiming to innovate in drug discovery and development.

Synonyms
Boc-Acpo-OH
CAS Number
882847-09-8
Purity
≥ 99% (HPLC)
Molecular Formula
C12H16N2O5
Molecular Weight
268.27
MDL Number
MFCD06656433
PubChem ID
2755970
Melting Point
173-178 °C
Appearance
White powder
Conditions
Store at 0-8 °C
General Information
Synonyms
Boc-Acpo-OH
CAS Number
882847-09-8
Purity
≥ 99% (HPLC)
Molecular Formula
C12H16N2O5
Molecular Weight
268.27
MDL Number
MFCD06656433
PubChem ID
2755970
Melting Point
173-178 °C
Appearance
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

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

  • Pharmaceutical Development: This compound serves as a key intermediate in the synthesis of various pharmaceuticals, particularly in the development of drugs targeting neurological disorders.
  • Bioconjugation: It is employed in bioconjugation processes, allowing researchers to attach biomolecules to surfaces or other molecules, enhancing drug delivery systems and diagnostic tools.
  • Peptide Synthesis: The compound is useful in peptide synthesis, providing a protective group that facilitates the assembly of complex peptides with improved stability and bioactivity.
  • Research in Medicinal Chemistry: It plays a significant role in medicinal chemistry research, aiding in the design of novel compounds with potential therapeutic effects, particularly in oncology.
  • Analytical Chemistry: This chemical is utilized in analytical methods for detecting and quantifying specific biomolecules, contributing to advancements in biochemical analysis and quality control.

Citations