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reactions. In this way, triisopropylbenzenes are converted back to diisopropylbenzenes upon treatment with benzene or monoisopropylbenzene. As usual, these transformations are catalyzed by
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Schmidt, Roland; Griesbaum, Karl; Behr, Arno; Biedenkapp, Dieter; Voges, Heinz-Werner; Garbe, Dorothea; Paetz, Christian; Collin, Gerd; Mayer, Dieter; Höke, Hartmut (2014). "Hydrocarbons".
569:
Wang LY, Guo QJ, Lee MS (9 August 2018). "Recent advances in metal extraction improvement: Mixture systems consisting of ionic liquid and molecular extractant".
716:
626:
553:
486:
The 1,3- and 1,4- isomers are mainly of interest as precursors to the respective dihydroxylbenzene derivatives, which exploits the
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53:. Three isomers exist: 1,2- 1,3-, and 1,4-diisopropylbenzene. All are colorless liquids, immiscible in water, with similar
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494:, as is implicit in the Hock rearrangement, which are of interest as radical initiators for
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Vora BV, Kocal JA, Barger PT, Schmidt RJ, Johnson JA (2003).
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at position 2 (taken as position 1 in the propofol molecule)
16:
Hydrocarbon compound; benzene ring with two isopropyl groups
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Schmiedel, Klaus W.; Decker, Daniel (2011). "Resorcinol".
79:) substituents. DIPB has been referred to as "a common
538:Kirk-Othmer Encyclopedia of Chemical Technology
701:Ullmann's Encyclopedia of Industrial Chemistry
611:Ullmann's Encyclopedia of Industrial Chemistry
425:They can also be prepared and transformed by
8:
688:Institute for Occupational Safety and Health
669:Institute for Occupational Safety and Health
650:Institute for Occupational Safety and Health
546:10.1002/0471238961.0112112508011313.a01.pub2
414:These alkylations are catalyzed by various
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313:Diisopropylbenzenes typically arise by
571:Separation and Purification Technology
540:. Vol. 2. John Wiley & Sons.
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299:0.072 mg·l in water (25 °C)
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302:Practically insoluble in water
296:Very slightly soluble in water
1:
709:10.1002/14356007.a23_111.pub2
619:10.1002/14356007.a13_227.pub3
583:10.1016/j.seppur.2018.08.016
510:, which is 1,3-DIPB with a
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490:. All three isomers form
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57:. They are classified are
684:GESTIS Substance Database
665:GESTIS Substance Database
646:GESTIS Substance Database
253:
240:
221:
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309:Production and reactions
111:1,4-Diisopropylbenzene
107:1,3-Diisopropylbenzene
103:1,2-Diisopropylbenzene
420:aluminium trichloride
744:at Wikimedia Commons
134:-Diisopropylbenzene
763:Isopropyl compounds
742:Diisopropylbenzenes
488:Hock rearrangements
128:-Diisopropylbenzene
122:-Diisopropylbenzene
94:Diisopropylbenzenes
21:diisopropylbenzenes
573:(Review article).
140:Chemical structure
64:bearing a pair of
740:Media related to
613:. pp. 1–74.
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30:with the formula
28:organic compounds
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319:isopropylbenzene
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218:Chemical formula
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100:Systematic name
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55:boiling points
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534:"Alkylation"
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116:Common name
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83:" alongside
62:hydrocarbons
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18:
577:: 292–303.
431:Lewis acids
416:Lewis acids
752:Categories
519:References
418:, such as
315:alkylation
292:Solubility
237:Molar mass
168:CAS Number
591:105020998
323:propylene
241:162.28 g/
189:CID 11345
178:100-18-5
66:isopropyl
508:Propofol
502:See also
207:CID 7486
198:CID 7450
172:577-55-9
59:aromatic
686:of the
682:in the
680:Record
667:of the
663:in the
661:Record
648:of the
644:in the
642:Record
466:→ 2 C
286:210 °C
283:203 °C
280:205 °C
270:−17 °C
267:−63 °C
264:−57 °C
254:Liquid
211:PubChem
202:PubChem
193:PubChem
184:PubChem
175:99-62-7
81:diluent
715:
625:
589:
552:
446:(CH(CH
398:(CH(CH
85:hexane
40:(CH(CH
24:(DIPB)
587:S2CID
474:CH(CH
390:→ C
386:CH=CH
382:+ CH
374:CH(CH
354:CH(CH
346:→ C
342:CH=CH
338:+ CH
321:with
209:from
200:from
191:from
70:CH(CH
713:ISBN
623:ISBN
550:ISBN
458:+ C
87:.
26:are
19:The
705:doi
615:doi
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575:210
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243:mol
754::
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470:H
468:6
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462:H
460:6
456:2
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448:3
444:4
442:H
440:6
438:C
408:2
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396:4
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372:5
370:H
368:6
366:C
360:2
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352:5
350:H
348:6
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336:6
334:H
332:6
330:C
227:H
223:C
132:p
126:m
120:o
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68:(
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42:3
38:4
36:H
34:6
32:C
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