2,6-Diisopropylaniline
| Names | |
|---|---|
| Preferred IUPAC name
2,6-Di(propan-2-yl)aniline | |
| Other names
2,6-Diisopropylaniline
2,6-DIPA | |
| Identifiers | |
3D model (JSmol)
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| ChEMBL | |
| ChemSpider | |
| ECHA InfoCard | 100.042.081 |
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PubChem CID
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| UNII | |
CompTox Dashboard (EPA)
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| Properties | |
| C12H19N | |
| Molar mass | 177.291 g·mol−1 |
| Appearance | colorless liquid |
| Melting point | −45 °C (−49 °F; 228 K) |
| Boiling point | 257 °C (495 °F; 530 K) |
| Hazards | |
| GHS labelling: | |
| H412 | |
| P273, P501 | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references
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2,6-Diisopropylaniline is an organic compound with the formula H2NC6H3(CHMe2)2 (Me = CH3). It is a colorless liquid although, like many anilines, samples can appear yellow or brown. 2,6-Diisopropylaniline is a bulky aromatic amine that is often used to make ligands in coordination chemistry. The Schrock carbenes often are transition metal imido complexes derived from this aniline. Condensation with diacetylpyridine and acetylacetone gives, respectively, diiminopyridine and NacNac ligands.