For research use only. Not for therapeutic Use.
2-Thiophenecarboxaldehyde(Cat No.:R018387)is an aromatic heterocyclic aldehyde featuring a thiophene ring substituted at the 2-position with a formyl group. It is a valuable building block in organic synthesis, widely used in the development of pharmaceuticals, agrochemicals, dyes, and conducting polymers. Its reactive aldehyde functionality enables participation in condensation reactions, Schiff base formation, and heterocycle synthesis. The sulfur-containing thiophene core offers electron-rich aromatic character, making it suitable for designing π-conjugated systems. 2-Thiophenecarboxaldehyde is an essential intermediate for constructing complex molecules in research and industrial chemistry.
CAS Number | 98-03-3 |
Synonyms | 2-Formylthiofuran; 2-Formylthiophene; 2-Thienaldehyde; 2-Thienylaldehyde; 2-Thienylcarbaldehyde; 2-Thienylcarboxaldehyde; 2-Thiofurancarboxaldehyde; 2-Thiophenealdehyde; NSC 2162; Thiofurfural; Thiophene-2-carbaldehyde; Thiophene-2-carboxaldehyde; Th |
Molecular Formula | C5H4OS |
Purity | ≥95% |
Target | Endogenous Metabolite |
Storage | -20°C |
IUPAC Name | thiophene-2-carbaldehyde |
InChI | InChI=1S/C5H4OS/c6-4-5-2-1-3-7-5/h1-4H |
InChIKey | CNUDBTRUORMMPA-UHFFFAOYSA-N |
SMILES | C1=CSC(=C1)C=O |
Chemistry Calculators | Dilution Calculator In vivo Formulation Calculator Molarity Calculator Molecular Weight Calculator Reconstitution Calculator |