| Weight | 134.222 g/mol |
|---|---|
| Formula | C10H14 |
| Hydrogen Acceptors | 0 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 1 |
O-CYMENE (527-84-4)
1-methyl-2-isopropylbenzene · o-cymol · ortho-cymol
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- Arene ruthenium complexes of N,N- and N,O-donor schiff base ligands: an X-ray structure of [(6-p-cymene) RuCl(C5,H4N-2-CHNC6H4-p-Me)ClC6H6H2O (Polyhedron, 1992)
- Synthesis, Structures, and Norbornene ROMP Behavior of o-Aryloxide-N-Heterocyclic Carbene p-Cymene Ruthenium Complexes (Organometallics, 2012)
- Tellurated Schiff Bases Formed from {2-[(4-Methoxyphenyl)telluro]ethyl}amine and Bis(2-aminoethyl) Telluride with o-Hydroxyacetophenone: Synthesis and Complexation Reactions with HgII, PdII and RuII Crystal Structures of the Ligands, [Ru(p-cymene)Cl{H2NCH2CH2TeC6H4-4-OCH3}]ClH2O and [RuCl{4-MeOC6H4TeCH2CH2NHCH(CH3)C6H4-2-O}] (European Journal of Inorganic Chemistry, 2004)
- An eta^2-Aryl-Metal Interaction Turns a Chiral Monodentate Phosphoramidite into a Chelating Ligand in (S~a,S~R~u,R~c,R~c)-[RuCl(eta^6-p-cymene) (O,O'-(1,1'-dinaphthyl-2,2'-diyl)-N-(1-(1,2-eta-1-naphthyl)ethyl)-N-(1-(1-naphthyl)ethyl)phosphoramidite-kappaP)]PF~6 (Organometallics, 2005)
- o-Aryloxide-N-heterocyclic Carbenes: Efficient Synthesis of the Proligands and Their p-Cymene Ruthenium Complexes (Organometallics, 2015)
- Synthesis of o,m-cymene-cored biaryls through a carbanion-induced ring transformation strategy (Tetrahedron Letters, 2006)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - 1-methyl-2-isopropylbenzene
- o-cymol
- ortho-cymol
-
SMILESCC1=CC=CC=C1C(C)C
-
InChIKeyWWRCMNKATXZARA-UHFFFAOYSA-N
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