3-Ethoxypyridin-2-amine
CAS No.:
10006-74-3
M. Wt:
138.16700
M. Fa:
C7H10N2O
InChI Key:
ASJVXZBTTFDZDW-UHFFFAOYSA-N
Appearance:
Pale-yellow Solid
Names and Identifiers of 3-Ethoxypyridin-2-amine
CAS Number |
10006-74-3 |
|---|---|
EC Number |
808-783-8 |
MDL Number |
MFCD00234961 |
IUPAC Name |
3-ethoxypyridin-2-amine |
InChI |
InChI=1S/C7H10N2O/c1-2-10-6-4-3-5-9-7(6)8/h3-5H,2H2,1H3,(H2,8,9) |
InChIKey |
ASJVXZBTTFDZDW-UHFFFAOYSA-N |
Canonical SMILES |
CCOC1=C(N=CC=C1)N |
UNSPSC Code |
12352100 |
Physical and chemical properties of 3-Ethoxypyridin-2-amine
Boiling Point |
249.6ºC at 760mmHg |
|---|---|
Density |
1.101g/cm3 |
Exact Mass |
138.07900 |
Flash Point |
104.7ºC |
Index of Refraction |
1.548 |
LogP |
1.64370 |
Molecular Formula |
C7H10N2O |
Molecular Weight |
138.16700 |
PSA |
48.14000 |
Vapour Pressure |
0.0227mmHg at 25°C |
Safety Information of 3-Ethoxypyridin-2-amine
Applications of 3-Ethoxypyridin-2-amine
3-Ethoxypyridin-2-amine has several potential applications:
- Pharmaceuticals: It serves as a building block in the synthesis of various pharmaceutical agents.
- Agricultural Chemicals: Due to its biological activity, it may find use in developing agrochemicals.
- Research Tools: It can be utilized in biochemical assays to explore enzyme interactions and mechanisms.
Interaction Studies of 3-Ethoxypyridin-2-amine
Interaction studies involving 3-Ethoxypyridin-2-amine focus on its binding affinity to various biological targets. These studies help elucidate its mechanism of action and potential side effects:
- Protein-Ligand Binding: Investigations into how this compound interacts with proteins can reveal insights into its therapeutic potential.
- Metabolic Pathway Analysis: Understanding how it is metabolized within biological systems informs safety and efficacy profiles.
Biological Activity of 3-Ethoxypyridin-2-amine
The biological activity of 3-Ethoxypyridin-2-amine is of significant interest. Preliminary studies suggest that it may exhibit:
- Antimicrobial Properties: Compounds containing pyridine rings are often explored for their antimicrobial effects.
- Anticancer Activity: Some derivatives have shown promise in inhibiting cancer cell proliferation.
- Enzyme Inhibition: It may act as an inhibitor for specific enzymes involved in metabolic pathways, potentially providing therapeutic benefits in conditions like non-alcoholic fatty liver disease.
Physical sample testing spectrum (NMR) of 3-Ethoxypyridin-2-amine
