72459-53-1 Usage
Molecular structure
Consists of an imidazole ring and an isoindole-1,3-dione ring connected by a 2-ethyl group.
Unique chemical compound
The combination of these two rings and the 2-ethyl group makes it a distinct compound with potential applications in various fields.
Potential use in pharmaceutical research
Due to its structural similarity to certain biologically active molecules, it can interact with biological receptors, making it a candidate for drug development.
Structural similarity to biologically active molecules
This feature allows the compound to potentially mimic or modulate the activity of other molecules, which can be useful in creating new medications.
Interaction with biological receptors
The compound's ability to bind to and interact with biological receptors can lead to the development of new therapeutic agents.
Applications in organic synthesis
The diverse functional groups and reactivity of the compound make it a valuable building block for creating new organic molecules.
Material science applications
The compound's unique properties may be harnessed for the development of new materials with specific characteristics.
Need for further research and experimentation
To fully understand the potential uses and properties of 2-(2-IMIDAZOL-1-YL-ETHYL)-ISOINDOLE-1,3-DIONE, more studies and tests must be conducted.
Check Digit Verification of cas no
The CAS Registry Mumber 72459-53-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,4,5 and 9 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 72459-53:
(7*7)+(6*2)+(5*4)+(4*5)+(3*9)+(2*5)+(1*3)=141
141 % 10 = 1
So 72459-53-1 is a valid CAS Registry Number.
InChI:InChI=1/C13H11N3O2/c17-12-10-3-1-2-4-11(10)13(18)16(12)8-7-15-6-5-14-9-15/h1-6,9H,7-8H2
72459-53-1Relevant articles and documents
AN UNUSUAL AMINAL DERIVATIVE FROM A MISDIRECTED GABRIEL SYNTHESIS
Press, J. B.,Haug, M. F.,Wright, W. B.
, p. 837 - 842 (2007/10/02)
N-(2-bromoethyl)phthalimide (1) was reacted with sodium imidazolate in DMF to give the novel aminal N-phthalimide (4a) as well as N-vinylphthalimide (3) and the desired Gabriel intermediate 2.Aminal 4a as well as heterologues 4b - d form directly from rection of 3 with the appropriate heterocyclic sodium salt.
