| Weight | 210.039 g/mol |
|---|---|
| Formula | C4H3IS |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 0 |
2-IODOTHIOPHENE (3437-95-4)
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- 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)
- Plasma polymerization of 2-iodothiophene (Chemistry of Materials, 1996)
- Thin conductive coatings formed by plasma polymerization of 2-iodothiophene (Surface & Coatings Technology, 1993)
- Near ultraviolet photochemistry of 2-bromo- and 2-iodothiophene: Revealing photoinduced ring opening in the gas phase? (Journal of Chemical Physics, 2015)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CSC(=C1)I
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InChIKeyROIMNSWDOJCBFR-UHFFFAOYSA-N
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2-IODOTHIOPHENE
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