Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references
Chemical compound
1,3-Diiminoisoindoline is a dye precursor used in industry.[2] The molecule can exist in different tautomers resulting in different crystalline solids.[3]
^ abCID 18980 from PubChem
^Venkataraman, K. (2 December 2012). The Chemistry of Synthetic Dyes. Elsevier. pp. 283–311. ISBN 9780323142953.
^Zhang, Zhi-Qin; Njus, Jeffrey M.; Sandman, Daniel J.; Guo, Chengyun; Foxman, Bruce M.; Erk, Peter; van Gelder, Richard (2004). "Diiminoisoindoline: tautomerism, conformations, and polymorphism". Chemical Communications (7): 886–7. doi:10.1039/B400111G. PMID 15045113.
Diiminoisoindole Names IUPAC name 3-Iminoisoindol-1-amine Other names Isoindoline-1,3-diimine; Phthalimide diimide Identifiers CAS Number 3468-11-9 3D...
compound is prepared by addition of ammonia to phthalonitrile to give diiminoisoindole, which in turn condenses first with N-methylcyanoacetamide and then...
solvents. It is prepared by addition of ammonia to phthalonitrile to give diiminoisoindole, which in turn condenses with barbituric acid. K. Hunger. W. Herbst...
cyclotetramerization of various phthalic acid derivatives including phthalonitrile, diiminoisoindole, phthalic anhydride, and phthalimides. Alternatively, heating phthalic...
cyclization of maleonitriles. Cross-cyclization with phthalonitrile or diiminoisoindole derivatives is possible introducing a flexibile synthetic route that...