Ethyl 5-aminothiazole-2-carboxylate
CAS No.:
100114-63-4
M. Wt:
172.20500
M. Fa:
C6H8N2O2S
InChI Key:
IZCSREAMZDZVFW-UHFFFAOYSA-N
Appearance:
Solid
Names and Identifiers of Ethyl 5-aminothiazole-2-carboxylate
CAS Number |
100114-63-4 |
|---|---|
EC Number |
828-964-5 |
MDL Number |
MFCD20697238 |
IUPAC Name |
ethyl 5-amino-1,3-thiazole-2-carboxylate |
InChI |
InChI=1S/C6H8N2O2S/c1-2-10-6(9)5-8-3-4(7)11-5/h3H,2,7H2,1H3 |
InChIKey |
IZCSREAMZDZVFW-UHFFFAOYSA-N |
Canonical SMILES |
CCOC(=O)C1=NC=C(S1)N |
UNSPSC Code |
12352100 |
Physical and chemical properties of Ethyl 5-aminothiazole-2-carboxylate
Exact Mass |
172.03100 |
|---|---|
H Bond Acceptors |
3 |
H Bond Donors |
1 |
LogP |
1.48320 |
Molecular Formula |
C6H8N2O2S |
Molecular Weight |
172.20500 |
PSA |
93.45000 |
Storage condition |
2-8°C(protect from light) |
Safety Information of Ethyl 5-aminothiazole-2-carboxylate
Applications of Ethyl 5-aminothiazole-2-carboxylate
Ethyl 5-aminothiazole-2-carboxylate finds applications across various fields:
- Pharmaceutical Development: It serves as a precursor for synthesizing bioactive compounds.
- Agricultural Chemistry: Potential use in developing agrochemicals due to its antimicrobial properties.
- Biochemical Research: Utilized as a reagent in biochemical assays and studies involving enzyme interactions.
Interaction Studies of Ethyl 5-aminothiazole-2-carboxylate
Studies on the interactions of ethyl 5-aminothiazole-2-carboxylate with biological molecules indicate its potential as a lead compound in drug discovery. Interaction studies often focus on:
- Binding Affinity: Assessing how well the compound binds to target proteins or enzymes.
- Mechanism of Action: Understanding how it affects cellular processes or metabolic pathways.
These studies are crucial for determining its viability as a therapeutic agent.
Biological Activity of Ethyl 5-aminothiazole-2-carboxylate
Research indicates that ethyl 5-aminothiazole-2-carboxylate exhibits notable biological activities, including:
- Antimicrobial Properties: It has shown effectiveness against various bacterial strains.
- Anticancer Activity: Some studies suggest that derivatives of this compound may inhibit cancer cell proliferation.
- Enzyme Inhibition: It may act as an inhibitor for specific enzymes involved in metabolic pathways, which could be beneficial in drug development.