Chemistry:1,3-Diisopropylbenzene
From HandWiki
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| Names | |
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| Preferred IUPAC name
1,3-Di(propan-2-yl)benzene | |
| Other names
m-Diisopropylbenzene
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| Identifiers | |
3D model (JSmol)
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| Properties | |
| C12H18 | |
| Molar mass | 162.276 g·mol−1 |
| Appearance | Colorless liquid |
| Density | 0.8559 |
| Melting point | −63 °C (−81 °F; 210 K) |
| Boiling point | 203 °C (397 °F; 476 K) |
| 0.0425 g/L | |
| Hazards | |
| GHS pictograms |   
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| GHS Signal word | Warning |
| H335, H336, H361, H410 | |
| P201, P202, P261, P271, P273, P281, P304+340, P308+313, P312, P391, P403+233, P405, P501 | |
| 449 °C; 840 °F; 722 K | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
| Infobox references | |
Tracking categories (test):
1,3-Diisopropylbenzene is an aromatic hydrocarbon with the formula C6H4(CHMe2)2 (Me = CH3). It is one of three isomeric diisopropylbenzenes. This colorless liquid is prepared by thermal isomerization of 1,4-diisopropylbenzene over a solid acid catalyst.[1] It is the principal industrial precursor to resorcinol via the Hock rearrangement.[2]
References
- ↑ Corma, A.; Fornes, V.; Pergher, S. B.; Maesen, Th. L. M.; Buglass, J. G. (1998). "Delaminated Zeolite Precursors as Selective Acidic Catalysts". Nature 396 (6709): 353–356. doi:10.1038/24592. Bibcode: 1998Natur.396..353C.
- ↑ K. W. Schmiedel; D. Decker (2012). "Ullmann's Encyclopedia of Industrial Chemistry". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a23_111.pub2.
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