Talk:Isoindole

Tautomers
Both tautomers are aromatic, the one on the left with a 6 pi benzene ring, the one on the right is 10 pi aromatic. So, this page is in error and I have edited it.

Call me stupid, but isn't the pyrrole-like tautomer the one with aromacity around the whole ring system? So shouldn't isoindols chemical properties in solution be more Imine-like, which I doubt? So wouldn't it be right to say the one WITH full aromacity is dominant? But I'm not sure of that and I don't have a heterocycles-textbook around... —Preceding unsigned comment added by 91.47.86.194 (talk) 17:54, 13 May 2008 (UTC)


 * I have expanded the section about tautomers and added references to support the claims. ChemNerd (talk) 10:09, 23 May 2013 (UTC)

Is it poisonous? What is it used for?
Well? 2602:306:C518:6C40:F02A:330C:11CC:ACDB (talk) 00:07, 23 May 2013 (UTC)