81928-79-2 Usage
Uses
Used in Organic Synthesis:
1-(3-nitrophenyl)-N-[2-[(3-nitrophenyl)methylideneamino]ethyl]methanimine is utilized as an intermediate in organic synthesis, particularly for the creation of various complex organic molecules. Its unique structure allows for versatile reactions and the formation of a wide range of compounds.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 1-(3-nitrophenyl)-N-[2-[(3-nitrophenyl)methylideneamino]ethyl]methanimine is used as a key compound in the development of new drugs. Its properties and reactivity make it a valuable candidate for the synthesis of potential therapeutic agents, with ongoing research aimed at uncovering its full potential in this area.
Further research and investigations are being conducted to explore the compound's potential uses and properties, which may lead to additional applications in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 81928-79-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,9,2 and 8 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 81928-79:
(7*8)+(6*1)+(5*9)+(4*2)+(3*8)+(2*7)+(1*9)=162
162 % 10 = 2
So 81928-79-2 is a valid CAS Registry Number.
81928-79-2Relevant academic research and scientific papers
An abnormal C-H?O bond directs intermolecular bonding arrangements in bisimines
Reyes-Arellano, Alicia,Vega-Ramírez, Leticia,Nájera-Mundo, Jorge A.,Salgado-Zamora, Héctor,Molins, Elies,Peralta-Cruz, Javier,Tamariza, Joaquín
, p. 141 - 148 (2007/10/03)
N,N-bis(3-nitrobenzylidene)ethylenediamine (1) formed a supramolecule with meso-hydrobenzoin, whereas N,N-bis(4-nitrobenzylidene)ethylenediamine (2) underwent a self-assembling process. The X-ray diffraction analysis showed that C-H?O intermolecular conta
Studies about the cyclization of 1,2-diamines with aldehydes and ketones
Lessel
, p. 649 - 653 (2007/10/02)
The reaction of the 1,2-dinucleophile ethylendiamine with benzaldehydes yields diimines, from o-phenylendiamine monoimines respectively benzimidazoles are formed. β-Diketones give 1,5-benzodiazepines. The different behaviour is explained by MNDO calculati
