Glyoxal-bis(mesitylimine)
.svg.png) | |
| Names | |
|---|---|
| IUPAC name
2,4,6-Trimethyl-N-[(2E)-2-[(2,4,6-trimethylphenyl)imino]ethylidene]aniline | |
| Identifiers | |
| 56222-36-7 | |
| 3D model (Jmol) | Interactive image |
| ChemSpider | 2971578 |
| PubChem | 3741651 |
| |
| |
| Properties | |
| C20H24N2 | |
| Molar mass | 292.43 g·mol−1 |
| Appearance | Yellow solid |
| Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
| Infobox references | |
Glyoxal-bis(mesitylimine) is an organic compound with the formula H2C2(NC6H2Me3)2 (Me = methyl). It is a yellow solid that is soluble in organic solvents. It is classified as a diimine ligand. It is used in coordination chemistry and homogeneous catalysis. It is synthesized by condensation of 2,4,6-trimethylaniline and glyoxal.[1]
References
- ↑ Ison, Elon A.; Ison, Ana (2012). "Synthesis of Well-Defined CopperN-Heterocyclic Carbene Complexes and Their Use as Catalysts for a "Click Reaction": A Multistep Experiment That Emphasizes the Role of Catalysis in Green Chemistry". Journal of Chemical Education: 121010095600000. doi:10.1021/ed300243s.
This article is issued from Wikipedia - version of the 12/1/2016. The text is available under the Creative Commons Attribution/Share Alike but additional terms may apply for the media files.