Ethyl 4-formylthiophene-3-carboxylate
CAS No.:
67808-74-6
M. Wt:
184.212
M. Fa:
C8H8O3S
InChI Key:
NIWFVGVEYJQBOT-UHFFFAOYSA-N
Names and Identifiers of Ethyl 4-formylthiophene-3-carboxylate
CAS Number |
67808-74-6 |
|---|---|
MDL Number |
MFCD28125618 |
IUPAC Name |
ethyl 4-formylthiophene-3-carboxylate |
InChI |
InChI=1S/C8H8O3S/c1-2-11-8(10)7-5-12-4-6(7)3-9/h3-5H,2H2,1H3 |
InChIKey |
NIWFVGVEYJQBOT-UHFFFAOYSA-N |
Canonical SMILES |
CCOC(=O)C1=CSC=C1C=O |
UNSPSC Code |
12352100 |
Physical and chemical properties of Ethyl 4-formylthiophene-3-carboxylate
Boiling Point |
304.5±27.0 °C at 760 mmHg |
|---|---|
Density |
1.3±0.1 g/cm3 |
Exact Mass |
184.019409 |
Flash Point |
137.9±23.7 °C |
Index of Refraction |
1.573 |
LogP |
0.93 |
Molecular Formula |
C8H8O3S |
Molecular Weight |
184.212 |
Storage condition |
2-8°C |
Vapour Pressure |
0.0±0.6 mmHg at 25°C |
Safety Information of Ethyl 4-formylthiophene-3-carboxylate
Applications of Ethyl 4-formylthiophene-3-carboxylate
Ethyl 4-formylthiophene-3-carboxylate has various applications in:
- Organic Synthesis: It serves as a building block for synthesizing more complex organic molecules.
- Pharmaceutical Development: Due to its potential biological activity, it can be explored for developing new antimicrobial agents or other therapeutic compounds.
- Material Science: Its derivatives may find utility in creating functional materials with electronic or optical properties.
Biological Activity of Ethyl 4-formylthiophene-3-carboxylate
Recent studies have indicated that derivatives of ethyl 4-formylthiophene-3-carboxylate exhibit significant biological activities. For instance, azomethines derived from similar thiophene compounds have shown antibacterial properties against Gram-positive bacteria. The unique structure of ethyl 4-formylthiophene-3-carboxylate may enhance its bioactivity, making it a candidate for further pharmacological studies.