60025-39-0 Usage
Uses
Used in Pharmaceutical Applications:
1-(4-[(1E)-2-(4-acetylphenyl)-2,3-dihydro-1H-isoindol-1-ylidene]aminophenyl)ethanone is used as a pharmaceutical compound for the development of drugs targeting various diseases. Its complex structure and functional group provide a foundation for creating novel therapeutic agents.
Used in Organic Synthesis:
In the field of organic chemistry, 1-(4-[(1E)-2-(4-acetylphenyl)-2,3-dihydro-1H-isoindol-1-ylidene]aminophenyl)ethanone is used as a versatile building block for the synthesis of other organic molecules. Its aromatic and aliphatic structures offer potential for creating a wide range of compounds with diverse applications.
Used in Research and Development:
1-(4-[(1E)-2-(4-acetylphenyl)-2,3-dihydro-1H-isoindol-1-ylidene]aminophenyl)ethanone is utilized in research and development for studying its interactions with other substances and its behavior in different environments. 1-(4-[(1E)-2-(4-acetylphenyl)-2,3-dihydro-1H-isoindol-1-ylidene]aminophenyl)ethanone's potential is still being explored, and further study is necessary to understand its full capabilities and applications.
Check Digit Verification of cas no
The CAS Registry Mumber 60025-39-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,0,2 and 5 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 60025-39:
(7*6)+(6*0)+(5*0)+(4*2)+(3*5)+(2*3)+(1*9)=80
80 % 10 = 0
So 60025-39-0 is a valid CAS Registry Number.
60025-39-0Relevant academic research and scientific papers
Synthesis of mixed N,N′-(Ar,Ar′-diaryl)iminoisoindolines for applications in palladacycle formations
Chitanda, Jackson M.,Wu, Shih-Chang,Wilson Quail,Foley, Stephen R.
experimental part, p. 122 - 129 (2012/02/02)
The synthesis of N,N′-(Ar,Ar′-diaryl)iminoisoindolines containing different aryl groups bound to the two nitrogen atoms is described. The iminoisoindolines were obtained by a three component, one-pot reaction of phthalaldehyde with 1 equivalent p-NO2
Synthesis of palladacycles employing iminoisoindolines as monoanionic bidentate ligands
Chitanda, Jackson M.,Prokopchuk, Demyan E.,Quail, J. Wilson,Foley, Stephen R.
experimental part, p. 6023 - 6029 (2009/02/08)
A series of air- and moisture-stable iminoisoindoline-based palladacycles have been prepared in two operationally simple steps from commercially available reagents. para-Substituted N,N′-diphenyliminoisoindoline ligands are easily synthesized from phthalaldehyde and para-substituted anilines and further reaction of the iminoisoindoline ligands with Pd(OAc)2 in dichloromethane at room temperature results in formation of six-membered [C,N] dinuclear cyclopalladated complexes with the general formula [(iminoisoindoline)Pd(μ-OAc)]2. The resulting palladacyclic complexes were tested as precatalysts in Heck and Suzuki coupling reactions.
