104830-22-0 Usage
General Description
The chemical compound (1Z)-1-[(4-methoxyphenyl)imino]-1H-isoindol-3-amine, also known as 4-Methoxyphenyl)imino)-1H-isoindol-1-amine, is an organic compound with the molecular formula C15H13N3O. It is a derivative of isoindole, which is a bicyclic aromatic compound. (1Z)-1-[(4-methoxyphenyl)imino]-1H-isoindol-3-amine contains a methoxy group and an imine group, and it exhibits a yellowish-brown color. It is commonly used in organic synthesis and pharmaceutical research due to its potential biological activity. Additionally, it has been investigated for its potential applications in the field of material science and as a building block for the synthesis of various organic compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 104830-22-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,8,3 and 0 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 104830-22:
(8*1)+(7*0)+(6*4)+(5*8)+(4*3)+(3*0)+(2*2)+(1*2)=90
90 % 10 = 0
So 104830-22-0 is a valid CAS Registry Number.
104830-22-0Relevant 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.
Spiessens, Luc I.,Anteunis, M. J. O.
, p. 431 - 452 (2007/10/02)
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.
