Weight | 112.197 g/mol |
---|---|
Formula | C6H8S |
Hydrogen Acceptors | 1 |
Hydrogen Donors | 0 |
Aromatic Rings | 1 |
Rotatable Bonds | 0 |
3,4-Dimethylthiophene (632-15-5)
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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)
- 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)
- Investigation into the reaction of 2-amino-4,5-dimethylthiophene-3-carboxamide with iso(and isothio)cyanates under microwave irradiation (Heteroatom Chemistry, 2009)
- Hydrogenation of (1-phenylthiophene)Mn(CO)3 (thiophene=3-methylthiophene and 3,4-dimethylthiophene) complexes: formation of tetrakis(tricarbonyl-phenylthiomanganese) (Journal of Organometallic Chemistry, 1999)
- Reactions of the iridathiabenzene complex Cp{sup *}Ir(2,5-dimethylthiophene) with Co{sub 2}(CO){sub 8}, Co{sub 4}(CO){sub 12}, and ({eta}{sup 6}-C{sub 6}H{sub 3}Me{sub 3})Co{sub 4}(CO){sub 9} (Organometallics, 1996)
- Copper (I) catalysed formation of 3-Methoxy-2,5-dimethylthiophene and 3,4-dimethoxy-2,5-dimethylthiophene (Tetrahedron, 1994)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCC1=CSC=C1C
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InChIKeyGPSFYJDZKSRMKZ-UHFFFAOYSA-N
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