| Weight | 112.153 g/mol |
|---|---|
| Formula | C5H4OS |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 1 |
3-Thiophenecarboxaldehyde (498-62-4)
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- Synthesis of 3,2':5',3"-terthiophene and other terthiophenes by the thiophenecarboxaldehyde .fwdarw. ethynylthiophene .fwdarw. dithienylbutadiyne route (Journal of Organic Chemistry, 1982)
- Synthesis, spectroscopic studies and crystal structure of the Schiff base ligand L derived from condensation of 2-thiophenecarboxaldehyde and 3,3'-diaminobenzidine and its complexes with Co(II), Ni(II), Cu(II), Cd(II) and Hg(II): Comparative DNA binding studies of L and its Co(II), Ni(II) and Cu(II) complexes. (Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy, 2011)
- A SHORT, PRACTICAL SYNTHESIS OF 3-THIOPHENECARBOXALDEHYDE (Synthetic Communications, 2001)
- Chemistry of Thiophene. I. Derivatives of 3-Thiophenecarboxaldehyde (Journal of Organic Chemistry, 1957)
- Theoretical Studies of Solid-State Reactivity by Packing Density and Potential-Energy Maps: Hydrogen Transfer in 5-Nitro-3-thiophenecarboxaldehyde Crystals (Acta Crystallographica Section B-structural Science, 1987)
- Synthesis and some reactions of sulfides of the thiophene series: Communication 6. Action of sodium in liquid ammonia on acetals of 2-(ethylthio)- and 2-(benzylthio)-5-ethyl-3-thiophenecarboxaldehyde (Russian Chemical Bulletin, 1962)
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Predict GHS Hazards for Any Chemical in silico.
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SMILESC1=CSC=C1C=O
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InChIKeyRBIGKSZIQCTIJF-UHFFFAOYSA-N
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