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Isoindolin
ββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββ
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Isoindolin ist eine chemische Verbindung aus der Gruppe der Heterocyclen.
Contents
β’ Eigenschaften
β’ Verwendung
β’ Einzelnachweise
ββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββββ
Gewinnung und Darstellung
Isoindolin kann aus PhthalsΓ€ureanhydrid mit Harnstoff ΓΌber Isoindolinon gewonnen werden.cite-ref-c-a-heaton-3-0[3]
Bornstein stellte Isoindolin durch hydrolytische Spaltung von 2-(p-Tolylsulfonyl)-isoindolin (hergestellt aus o-Xylylendibromid und p-Toluolsulfonamid) mit Phenol und BromwasserstoffsΓ€ure in PropionsΓ€ure her.cite-ref-doi10-1002-jps-2600530840-1-1[1]
Eigenschaften
Verwendung
Einzelnachweise
cite-note-doi10-1002-jps-2600530840-11. John L. Neumeyer: Facile Synthesis of Isoindoline and Substituted Isoindolines. In: Journal of Pharmaceutical Sciences. 53, 1964, S. 981, doi:10.1002/jps.2600530840.
cite-note-sigma-21. Datenblatt Isoindolin, 97% bei Sigma-Aldrich, abgerufen am 11. August 2018 (PDF).
cite-note-c-a-heaton-33. β C.A. Heaton: The Chemical Industry. Springer Science & Business Media, 2012, ISBN 978-94-011-1318-2, S. 170 (eingeschrΓ€nkte Vorschau in der Google-Buchsuche).
cite-note-willy-herbst-klaus-hunger-44. β Willy Herbst, Klaus Hunger: Industrielle Organische Pigmente. John Wiley & Sons, 2009, ISBN 3-527-62496-1, S. 418 (eingeschrΓ€nkte Vorschau in der Google-Buchsuche).