| Weight | 134.222 g/mol |
|---|---|
| Formula | C10H14 |
| Hydrogen Acceptors | 0 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 1 |
M-CYMENE (535-77-3)
1-methyl-3-isopropylbenzene
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- Room-temperature cyclometallation of amines, imines and oxazolines with [MCl2Cp*]2(M = Rh, Ir) and [RuCl2(p-cymene)]2 (Dalton Transactions, 2003)
- Mechanistic Study of Acetate-Assisted CH Activation of 2-Substituted Pyridines with [MCl2Cp*]2 (M = Rh, Ir) and [RuCl2(p-cymene)]2 (Organometallics, 2009)
- The 16-electron dithiolene complexes (p-cymene)M[S2C2(B10H10)] (M=Ru, Os) containing both 6-(p-cymene) and 2-(ortho-carborane-dithiolate): adduct formation with Lewis bases, and X-ray crystal structures of (p-cymene)Ru[S2C2(B10H10)](L) (L=PPh3) and {(p-cymene)Ru[S2C2(B10H10)]}2(-LL) (LL=Ph2PCH2CH2PPh2 and N2H4) (Journal of Organometallic Chemistry, 2000)
- Synthesis, interconversion, and structural characterization of the closo and nido clusters [(p-cymene)3M3S2]2+ and [p-cymene)3M3S2]0 (M = ruthenium, osmium) (Journal of the American Chemical Society, 1989)
- Room-temperature cyclometallation of amines, imines and oxazolines with [MCl2Cp*]2 (M = Rh, Ir) and [RuCl2(p-cymene)]2Based on the presentation given at Dalton Discussion No. 6, 9?11th September 2003, University of York, UK.Electronic supplementary information (ESI) available: Characterisation and crystallographic data for [IrCl2(NH2Ph)Cp*] (6), and Figures showing the structures of 3b, 5b and 6. See http://www.rsc.org/suppdata/dt/b3/b303737a/ (Dalton Transactions, 2003)
- Synthesis, Characterization, and Theoretical Studies on Heterobinuclear (p-cymene)Os(-pz)2M (M = Ir, Rh; Hpz = Pyrazole) Complexes (Organometallics, 2000)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - 1-methyl-3-isopropylbenzene
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SMILESCC1=CC(=CC=C1)C(C)C
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InChIKeyXCYJPXQACVEIOS-UHFFFAOYSA-N
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