| Weight | 112.197 g/mol |
|---|---|
| Formula | C6H8S |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 0 |
2,5-DIMETHYLTHIOPHENE (638-02-8)
Score:
#6785 in Chemistry
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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)
- Reactions of Cp*Ir(2,5-dimethylthiophene) with iron carbonyls : a new mechanism for thiophene hydrodesulfurization (Journal of the American Chemical Society, 1991)
- -Facial diastereoselectivity in Diels-Alder reactions of 2,5-dimethylthiophene oxide (Tetrahedron Letters, 1989)
- Desulfurization of thiophenic compounds by Ni(111): Adsorption and reactions of thiophene, 3-methylthiophene, and 2,5-dimethylthiophene (The Journal of Physical Chemistry, 1996)
- Reactions of the 2-and 4-isomers of Cp Ir(2,5-dimethylthiophene) with phosphines, co and H2 (Polyhedron, 1990)
- Adsorption of thiophene and 2,5-dimethylthiophene on Au(1 1 1) from ethanol solutions (Surface Science, 2003)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCC1=CC=C(S1)C
-
InChIKeyGWQOOADXMVQEFT-UHFFFAOYSA-N
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2,5-DIMETHYLTHIOPHENE
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