N-(3-formylpyridin-2-yl)acetamide
Names and Identifiers of N-(3-formylpyridin-2-yl)acetamide
CAS Number |
54856-85-8 |
|---|---|
IUPAC Name |
N-(3-methanoylpyridin-2-yl)ethanamide |
Canonical SMILES |
CC(=O)NC1=C(C=CC=N1)C=O |
Physical and chemical properties of N-(3-formylpyridin-2-yl)acetamide
Molecular Formula |
C8H8N2O2 |
|---|---|
Molecular Weight |
164.16 |
Applications of N-(3-formylpyridin-2-yl)acetamide
N-(3-Formylpyridin-2-YL)acetamide finds applications across multiple domains:
- Organic Synthesis: As a building block for synthesizing more complex organic compounds.
- Medicinal Chemistry: Investigated for its potential as a pharmaceutical intermediate in developing new drugs.
- Material Science: Used in creating specialty chemicals and polymers due to its reactive functional groups.
- Biological Research: Studied for its effects on various biological systems and its potential therapeutic benefits .
Interaction Studies of N-(3-formylpyridin-2-yl)acetamide
Studies on N-(3-Formylpyridin-2-YL)acetamide's interactions with biological targets are crucial for understanding its mechanism of action. Research focuses on how the compound binds to proteins or enzymes, potentially altering their activity. Understanding these interactions aids in evaluating its efficacy as a drug candidate and its role in biochemical pathways .
Biological Activity of N-(3-formylpyridin-2-yl)acetamide
Research into the biological activity of N-(3-Formylpyridin-2-YL)acetamide indicates potential antimicrobial and anticancer properties. The compound's ability to interact with biological targets stems from its functional groups, which can form covalent bonds with nucleophilic sites on proteins and enzymes. This interaction may inhibit their activity, making it a subject of interest for drug development and therapeutic applications .