Propanamide,N-(2-methylphenyl)-
Names and Identifiers of Propanamide,N-(2-methylphenyl)-
CAS Number |
19343-15-8 |
|---|---|
IUPAC Name |
N-(2-methylphenyl)propanamide |
Canonical SMILES |
CCC(=O)NC1=CC=CC=C1C |
Physical and chemical properties of Propanamide,N-(2-methylphenyl)-
Boiling Point |
298.5ºC at 760mmHg |
|---|---|
Density |
1.051g/cm3 |
Exact Mass |
163.10000 |
Flash Point |
177.2ºC |
Index of Refraction |
1.556 |
LogP |
2.41650 |
Molecular Formula |
C10H13NO |
Molecular Weight |
163.21600 |
PSA |
29.10000 |
Vapour Pressure |
0.00126mmHg at 25°C |
Applications of Propanamide,N-(2-methylphenyl)-
N-(2-methylphenyl)propanamide finds applications across various fields:
- Medicinal Chemistry: Used as a building block in drug development due to its biological activity.
- Chemical Research: Serves as a reagent in organic synthesis and as a standard in analytical chemistry.
- Agricultural Chemistry: Investigated for potential use in agrochemicals.
Interaction Studies of Propanamide,N-(2-methylphenyl)-
Research into the interaction of N-(2-methylphenyl)propanamide with biological molecules has shown its ability to bind to specific enzymes and receptors. These interactions are critical for understanding its mechanism of action and potential therapeutic applications. Studies often focus on its role in modulating pain pathways and inflammation responses.
Biological Activity of Propanamide,N-(2-methylphenyl)-
N-(2-methylphenyl)propanamide exhibits notable biological activities, particularly in pharmacological contexts. It has been studied for its potential as an inhibitor of certain enzymes and receptors, making it relevant in medicinal chemistry. Its structure allows for interactions with biological targets, influencing pathways related to pain modulation and inflammation.
Cas:802294-64-0