| Weight | 210.039 g/mol |
|---|---|
| Formula | C4H3IS |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 0 |
3-Iodothiophene (10486-61-0)
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- PREPARATION OF 3-THIENYLZINC AND -MAGNESIUM HALIDE VIA OXIDATIVE ADDITION OF ACTIVE ZINC AND MAGNESIUM TO 3-IODOTHIOPHENE (Journal of Organic Chemistry, 1995)
- The Effects of Binding Ligand Variation on the Nickel Catalyzed Externally Initiated Polymerization of 2Bromo3hexyl5iodothiophene (Macromolecular Chemistry and Physics, 2009)
- Kinetic Study, by UVVis Spectroscopy, on the Strong Effect of LiCl on the Controlled Polymerization of 2-Bromo-3-hexyl-5-iodothiophene and 2-Iodo-3-hexyl-5-bromothiophene: Determination of the Propagation Rate Constants, Application to the Synthesis of High Molecular Weight Polydodecylthiophene (Macromolecules, 2011)
- On the Halogen-Metal Exchange Reaction between 2-Bromo-3-iodothiophene and Ethyllithium. (Acta Chemica Scandinavica, 1969)
- Synthesis of 4H-thieno[3,2-c]chromenes by intramolecular arylation of 4-aryloxy-methyl-5-iodothiophene-2-carbaldehydes (Chemistry of Heterocyclic Compounds, 2012)
- Microwave Spectrum and Nuclear Quadrupole Interaction of 3-Iodothiophene in the Excited Vibrational States (Journal of Molecular Spectroscopy, 1990)
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Predict GHS Hazards for Any Chemical in silico.
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SMILESC1=CSC=C1I
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InChIKeyWGKRMQIQXMJVFZ-UHFFFAOYSA-N
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