Methyl 2-methoxyquinoline-4-carboxylate
CAS No.:
115801-85-9
M. Wt:
217.22100
M. Fa:
C12H11NO3
InChI Key:
MCOOETCYPKUYLA-UHFFFAOYSA-N
Names and Identifiers of Methyl 2-methoxyquinoline-4-carboxylate
CAS Number |
115801-85-9 |
|---|---|
MDL Number |
MFCD25955997 |
IUPAC Name |
methyl 2-methoxyquinoline-4-carboxylate |
InChI |
InChI=1S/C12H11NO3/c1-15-11-7-9(12(14)16-2)8-5-3-4-6-10(8)13-11/h3-7H,1-2H3 |
InChIKey |
MCOOETCYPKUYLA-UHFFFAOYSA-N |
Canonical SMILES |
COC1=NC2=CC=CC=C2C(=C1)C(=O)OC |
UNSPSC Code |
12352100 |
Physical and chemical properties of Methyl 2-methoxyquinoline-4-carboxylate
Acidity coefficient |
0.99±0.50(Predicted) |
|---|---|
Boiling Point |
327.4±22.0 °C(Predicted) |
Density |
1?+-.0.06 g/cm3(Predicted) |
Exact Mass |
217.07400 |
LogP |
2.03000 |
Molecular Formula |
C12H11NO3 |
Molecular Weight |
217.22100 |
PSA |
48.42000 |
Safety Information of Methyl 2-methoxyquinoline-4-carboxylate
Applications of Methyl 2-methoxyquinoline-4-carboxylate
Methyl 2-methoxyquinoline-4-carboxylate has a range of applications in different fields:
- Pharmaceuticals: Its potential as an anticancer and antimicrobial agent makes it a candidate for drug development.
- Agriculture: Compounds with similar structures have been investigated for their use as pesticides or herbicides.
- Material Science: Quinoline derivatives are explored for their properties in organic electronics and as fluorescent materials.
Interaction Studies of Methyl 2-methoxyquinoline-4-carboxylate
Interaction studies involving methyl 2-methoxyquinoline-4-carboxylate focus on its binding affinity with biological targets such as enzymes or receptors. These studies help elucidate its mechanism of action and potential therapeutic effects. For instance, investigations into its interactions with P-glycoprotein suggest that modifications at specific positions on the quinoline ring can significantly influence its efflux inhibition properties, which is crucial in drug absorption and efficacy.
Biological Activity of Methyl 2-methoxyquinoline-4-carboxylate
Methyl 2-methoxyquinoline-4-carboxylate has been studied for its potential biological activities, including:
- Antioxidant Properties: Compounds within this class have shown significant antioxidant activity, which is valuable for preventing oxidative stress-related diseases.
- Anticancer Activity: Some derivatives have demonstrated cytotoxic effects against various cancer cell lines, making them candidates for further development as anticancer agents.
- Antimicrobial Activity: Quinoline derivatives are known for their antimicrobial properties, which could be relevant for developing new antibiotics.
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