(E)-methyl 4-methoxy-2-oxopent-3-enoate
CAS No.:
63808-28-6
M. Wt:
158.15200
M. Fa:
C7H10O4
InChI Key:
-
Names and Identifiers of (E)-methyl 4-methoxy-2-oxopent-3-enoate
CAS Number |
63808-28-6 |
|---|---|
IUPAC Name |
methyl 4-methoxy-2-oxidanylidene-pent-3-enoate |
Canonical SMILES |
CC(=CC(=O)C(=O)OC)OC |
Physical and chemical properties of (E)-methyl 4-methoxy-2-oxopent-3-enoate
Exact Mass |
158.05800 |
|---|---|
LogP |
0.27870 |
Molecular Formula |
C7H10O4 |
Molecular Weight |
158.15200 |
PSA |
52.60000 |
Applications of (E)-methyl 4-methoxy-2-oxopent-3-enoate
Methyl 4-methoxy-2-oxopent-3-enoate has several applications:
- Synthetic Intermediate: It serves as a valuable intermediate in organic synthesis for producing more complex molecules, including pharmaceuticals and agrochemicals.
- Flavoring Agent: Due to its pleasant aroma, it may find applications in the food industry as a flavoring agent.
- Biochemical Research: Its derivatives are used in biochemical research to study enzyme interactions and metabolic pathways.
Interaction Studies of (E)-methyl 4-methoxy-2-oxopent-3-enoate
Interaction studies involving methyl 4-methoxy-2-oxopent-3-enoate focus on its reactivity with various biological macromolecules:
- Enzyme Inhibition: Research indicates that certain derivatives may inhibit specific enzymes involved in metabolic processes, providing insights into their potential therapeutic uses.
- Binding Studies: Studies on the binding affinity of this compound to protein targets help elucidate its mechanism of action in biological systems.
Biological Activity of (E)-methyl 4-methoxy-2-oxopent-3-enoate
The biological activity of methyl 4-methoxy-2-oxopent-3-enoate is an area of ongoing research. Compounds with similar structures have shown potential in various biological applications, including:
- Antimicrobial Activity: Some derivatives exhibit antibacterial properties, which may be attributed to their ability to interfere with bacterial cell wall synthesis.
- Anti-inflammatory Effects: Certain analogs have demonstrated anti-inflammatory properties, making them candidates for further pharmacological studies.