2-Pentanone, 4-[(4-nitrophenyl)imino]-
Names and Identifiers of 2-Pentanone, 4-[(4-nitrophenyl)imino]-
CAS Number |
100060-84-2 |
|---|---|
IUPAC Name |
4-(4-nitrophenyl)iminopentan-2-one |
InChI |
InChI=1S/C11H12N2O3/c1-8(7-9(2)14)12-10-3-5-11(6-4-10)13(15)16/h3-6H,7H2,1-2H3 |
InChIKey |
KNBUYZVBVBGNPG-UHFFFAOYSA-N |
Canonical SMILES |
CC(=NC1=CC=C(C=C1)[N+](=O)[O-])CC(=O)C |
Physical and chemical properties of 2-Pentanone, 4-[(4-nitrophenyl)imino]-
Exact Mass |
220.08500 |
|---|---|
LogP |
3.18950 |
Molecular Formula |
C11H12N2O3 |
Molecular Weight |
220.22500 |
PSA |
75.25000 |
Applications of 2-Pentanone, 4-[(4-nitrophenyl)imino]-
2-Pentanone, 4-[(4-nitrophenyl)imino]- has several applications:
- Chemistry: Used as a reagent in organic synthesis and as a building block for more complex molecules.
- Biology: Investigated for its potential biological activities.
- Medicine: Explored for its use in drug development due to its unique chemical structure.
- Industry: Utilized in developing new materials and as a precursor for various chemical products.
Interaction Studies of 2-Pentanone, 4-[(4-nitrophenyl)imino]-
The mechanism of action of 2-Pentanone, 4-[(4-nitrophenyl)imino]- involves interactions with molecular targets such as enzymes and receptors. The nitrophenyl group can facilitate electron transfer reactions, while the imino group may form hydrogen bonds with biological molecules. These interactions are crucial for modulating enzymatic activity and influencing biological processes.
Biological Activity of 2-Pentanone, 4-[(4-nitrophenyl)imino]-
Research indicates that 2-Pentanone, 4-[(4-nitrophenyl)imino]- exhibits potential biological activity. It has been studied for its antimicrobial and anticancer properties. The presence of the nitrophenyl group may enhance its interaction with biological targets, potentially modulating enzyme activity and receptor interactions. These interactions are significant for developing therapeutic agents.