88988-84-5

Basic information

• Product Name: 1H-Isoindol-3-amine, N-(4-methoxyphenyl)-1-[(4-methoxyphenyl)imino]-, (Z)-
• CAS NO: 88988-84-5
• Molecular Formula: C22H19N3O2
• Molecular Weight: 357.412
• Mol File: 88988-84-5.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 1H-Isoindol-3-amine, N-(4-methoxyphenyl)-1-[(4-methoxyphenyl)imino]-, (Z)-(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-Isoindol-3-amine, N-(4-methoxyphenyl)-1-[(4-methoxyphenyl)imino]-, (Z)-(88988-84-5)
• EPA Substance Registry System: 1H-Isoindol-3-amine, N-(4-methoxyphenyl)-1-[(4-methoxyphenyl)imino]-, (Z)-(88988-84-5)

Safety Data

• Hazardous Substances Data: 88988-84-5(Hazardous Substances Data)

Upstream product

• 104-94-9 4-methoxy-aniline 
• 91-15-6 phthalonitrile 
• 3468-11-9 1-imino-1H-isoindol-3-amine 
• 21021-41-0 1,1,3-trichloro-1H-isoindole 
• 160956-25-2 isoindole-1,3-diylidenediamine 
• 104830-22-0 1--1,3-diiminoisoindoline 
• 99-09-2 3-nitro-aniline 

Relevant articles and documents

NMR STUDIES ON IMIDINES. VII. THE TAUTOMERISM OF MONO-N-ARYL SUBSTITUTED PHTHALIC IMIDINES. A 1H AND 13C NUCLEAR MAGNETIC RESONANCE STUDY.

1H and 13C NMR data indicate the presence of N-aryl substituted phthalic imidines to exist as 3-amino-1-N-arylimino-1H-isoindole compounds in DMSO-d6.In CDCl3 a tautomeric equilibrium mixture containing 20percent of the imino form is observed.The presence of a dimeric association through intramolecular H bonds is suggested.It is shown that intramolecular NH-N hydrogen bonds displace the tautomeric equilibrium toward the imino tautomer in 2-pyridyl substituted phthalic imidines.In the reaction product of phthalic imidine and 2,6-diaminopyridine, 11, two pairs of intramolecular NH-N hydrogen bonds result in the presence of both amino and imino tautomeric forms in the same molecular species.

TAUTOMERISM AND ISOMERISM IN 1,3-DIIMINOISOINDOLINE DERIVATIVES. I. PROTOTROPIC TAUTOMERISM AND Z,E-ISOMERIZATION OF 1,3-DIIMINOISOINDOLINE DERIVATIVES

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