• Abstract
• Full-Text PDF [135 KB]
• Supplement File 1
• Supplement File 2

• Article Statistics
• Google Scholar
• Order Reprints

• Cite this article
• Export to BibTeX
• Export to EndNote

• [+] on DOAJ
• Wölfel, S
• Berndt, F
• Friedrichs, J
• Haese, M
• Joostberends, J
• Masri, B
• Schnerre, R
• Wabnik, M
• Kunick, C
• [+] on Google Scholar
• Wölfel, S
• Berndt, F
• Friedrichs, J
• Haese, M
• Joostberends, J
• Masri, B
• Schnerre, R
• Wabnik, M
• Kunick, C
• [+] on PubMed
• Wölfel, S
• Berndt, F
• Friedrichs, J
• Haese, M
• Joostberends, J
• Masri, B
• Schnerre, R
• Wabnik, M
• Kunick, C

•  CiteULike
•  Facebook
•  Mendeley
•  Twitter

This article is

• freely available
• re-usable

Molbank 2012, 2012(4), M785; doi:10.3390/M785

Short Note

4,5,6,7-Tetrachloro-2-(1H-imidazol-2-yl)isoindoline-1,3-dione

Sebastian Wölfel, Frederik Berndt, Jessica Friedrichs, Michael Haese, Janine Joostberends, Bader Masri, Renate Schnerre, Maximilian Wabnik and Conrad Kunick*

Institut für Medizinische und Pharmazeutische Chemie, Technische Universität Braunschweig, Beethovenstraße 55, D-38106 Braunschweig, Germany

* Author to whom correspondence should be addressed.

Received: 30 August 2012 / Accepted: 7 November 2012 / Published: 9 November 2012

Download PDF Full-Text [135 KB, uploaded 9 November 2012 15:06 CET]

Abstract: 4,5,6,7-Tetrachloro-2-(1H-imidazol-2-yl)isoindoline-1,3-dione was obtained by reaction of 2-aminoimidazole with 3,4,5,6-tetrachlorophthalic anhydride in refluxing acetic acid.

Keywords: tetrachlorophthalimide; tetrachlorophthalic anhydride; 2-aminoimidazole

Supplementary Files

• Supplementary File 1:

  3D structure (MOL, 2 KB) Display in MOL Viewer

  3D structure generated by CORINA by Molecular Networks.

• Supplementary File 2:

  MOL-Document (MOL, 2 KB) Display in MOL Viewer

Article Statistics

Cite This Article