| Weight | 112.197 g/mol |
|---|---|
| Formula | C6H8S |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 0 |
2,3-Dimethylthiophene (632-16-6)
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- Synthesis, spectroscopic characterization, electrochemical behaviour, reactivity and antibacterial activity of some transition metal complexes with 2-(N-salicylideneamino)-3-carboxyethyl-4,5-dimethylthiophene. (Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy, 2008)
- Desulfurization of thiophenic compounds by Ni(111): Adsorption and reactions of thiophene, 3-methylthiophene, and 2,5-dimethylthiophene (The Journal of Physical Chemistry, 1996)
- Cyclopalladated N,N-dimethylthiophene-2- and -3-carboselenoamide derivatives (Inorganica Chimica Acta, 1992)
- 2,5-dimethylthiophene coordination to three metal centers in (. eta. sup 4 ,S-. mu. sub 3 -2,5-Me sub 2 T)(IrCp sup * )(Mo(CO) sub 2 Cp) sub 2 (Organometallics, 1990)
- The Signs of the Methyl-Methyl Spin Couplings in 2,3-Dimethylthiophene, 2,3-Dimethylfuran, and 3-Iodo-2,5-dimethylfuran. (Acta Chemica Scandinavica, 1966)
- Investigation into the reaction of 2-amino-4,5-dimethylthiophene-3-carboxamide with iso(and isothio)cyanates under microwave irradiation (Heteroatom Chemistry, 2009)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCC1=C(SC=C1)C
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InChIKeyBZYUMXXOAYSFOW-UHFFFAOYSA-N
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