(E)-3-(3-chloro-4-fluorophenyl)prop-2-enamide
CAS No.:
1000530-51-7
M. Wt:
199.61
M. Fa:
C9H7ClFNO
InChI Key:
-
Names and Identifiers of 1000530-51-7
CAS Number |
1000530-51-7 |
|---|---|
IUPAC Name |
(E)-3-(3-chloranyl-4-fluoranyl-phenyl)prop-2-enamide |
Canonical SMILES |
C1=CC(=C(C=C1/C=C/C(=O)N)Cl)F |
Physical and chemical properties of 1000530-51-7
Molecular Formula |
C9H7ClFNO |
|---|---|
Molecular Weight |
199.61 |
Applications of 1000530-51-7
The applications of (2E)-3-(3-chloro-4-fluorophenyl)prop-2-enamide span several fields:
- Pharmaceuticals: This compound may serve as a lead structure for developing new drugs targeting various diseases, particularly cancers.
- Agricultural Chemicals: Its antimicrobial properties could be harnessed in developing new pesticides or fungicides.
- Material Science: The compound's unique structural features may find applications in creating advanced materials with specific properties.
Interaction Studies of 1000530-51-7
Interaction studies involving (2E)-3-(3-chloro-4-fluorophenyl)prop-2-enamide focus on its binding affinity to biological macromolecules. Techniques such as:
- Molecular Docking: This computational method helps predict how the compound interacts with specific protein targets.
- In Vitro Assays: Laboratory tests assess the biological response of cells exposed to varying concentrations of the compound.
These studies are crucial for understanding the mechanisms underlying its biological activity and potential therapeutic uses.
Biological Activity of 1000530-51-7
(2E)-3-(3-chloro-4-fluorophenyl)prop-2-enamide exhibits significant biological activity. Research indicates that compounds with similar structures often show:
- Anticancer Properties: Many unsaturated amides have been evaluated for their ability to inhibit cancer cell proliferation.
- Antimicrobial Activity: The presence of halogen substituents often enhances antimicrobial efficacy against various pathogens.
- Enzyme Inhibition: This compound may interact with specific enzymes, potentially acting as a competitive inhibitor.