Diiminoisoindole

Diiminoisoindole
Names
	IUPAC name 3-Iminoisoindol-1-amine
	Other names Isoindoline-1,3-diimine; Phthalimide diimide[1]
Identifiers
CAS Number	3468-11-9 [1];
3D model (JSmol)	Interactive image;
ChemSpider	17919;
ECHA InfoCard	100.020.389
EC Number	222-426-8;
PubChem CID	18980;
CompTox Dashboard (EPA)	DTXSID0044658 ;
	InChI InChI=1S/C8H7N3/c9-7-5-3-1-2-4-6(5)8(10)11-7/h1-4H,(H3,9,10,11) Key: RZVCEPSDYHAHLX-UHFFFAOYSA-N;
	SMILES C1=CC=C2C(=C1)C(=NC2=N)N;
Properties
Chemical formula	C8H7N3
Molar mass	145.165 g·mol−1
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references

1,3-Diiminoisoindoline is a dye precursor used in industry.[2] The molecule can exist in different tautomers resulting in different crystalline solids.[3]

References

CID 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.

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[PubChem-1] CID 18980 from PubChem

[2] Venkataraman, K. (2 December 2012). The Chemistry of Synthetic Dyes. Elsevier. pp. 283–311. ISBN 9780323142953.

[3] 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.