32386-99-5 Usage
Molecular structure
2-[(4-methylbenzylidene)amino]-1H-isoindole-1,3(2H)-dione has a complex molecular structure, which includes a benzylidene amino group attached to an isoindole-1,3(2H)-dione core.
Derivative
It is a derivative of isoindole-1,3(2H)-dione, meaning it is a modified version of the parent compound with additional functional groups.
Benzylidene amino group
The compound contains a benzylidene amino group (a benzene ring connected to a nitrogen atom via a carbon atom), which contributes to its unique properties and potential applications.
Pharmaceutical research
The compound is also of interest in pharmaceutical research, as its unique structure and properties may lead to the development of new drugs or therapeutic agents.
Scientific interest
Its unique structure and properties make 2-[(4-methylbenzylidene)amino]-1H-isoindole-1,3(2H)-dione a subject of interest for scientists and researchers who are looking to explore its potential uses in various industries.
Molecular interactions
The ability of 2-[(4-methylbenzylidene)amino]-1H-isoindole-1,3(2H)-dione to interact with other molecules is of interest for further study, as these interactions may lead to new insights into its potential applications.
Biological activities
The potential biological activities of the compound make it a subject of interest for further study, as these activities may contribute to its potential use in pharmaceuticals or other industries.
Check Digit Verification of cas no
The CAS Registry Mumber 32386-99-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,2,3,8 and 6 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 32386-99:
(7*3)+(6*2)+(5*3)+(4*8)+(3*6)+(2*9)+(1*9)=125
125 % 10 = 5
So 32386-99-5 is a valid CAS Registry Number.
32386-99-5Relevant articles and documents
A convenient synthesis of 1-alkyl-1-phenylhydrazines from N-aminophthalimide
Nara, Shigeru,Sakamoto, Takeshi,Miyazawa, Etsuko,Kikugawa, Yasuo
, p. 87 - 98 (2007/10/03)
N-Alkylaminophthalimides were synthesized by condensation of N-aminophthalimide with aldehydes, and subsequent reduction of the intermediate with pyridine-borane in acetic acid. N-Phenylation and removal of the phthalimide group gave 1-alkyl-1-phenylhydrazines in high yield.
