5874-11-3 Usage
Description
1-(2,3-diphenylquinoxalin-6-yl)-3-(3-hydroxypropyl)urea is a chemical compound characterized by its molecular formula C26H24N4O2. It is a urea derivative featuring a quinoxaline ring and a hydroxypropyl side chain, which contribute to its potential pharmacological properties.
Uses
Used in Pharmaceutical Research and Drug Development:
1-(2,3-diphenylquinoxalin-6-yl)-3-(3-hydroxypropyl)urea is utilized as a compound in pharmaceutical research and drug development due to its potential pharmacological properties. Its unique structure may offer various applications in the treatment of different diseases, although further research is necessary to fully comprehend its biological activity and potential therapeutic uses.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 1-(2,3-diphenylquinoxalin-6-yl)-3-(3-hydroxypropyl)urea serves as a valuable compound for the design and synthesis of new drugs. Its structural features can be exploited to develop novel therapeutic agents targeting a range of medical conditions.
Used in Chemical Synthesis:
1-(2,3-diphenylquinoxalin-6-yl)-3-(3-hydroxypropyl)urea is also used as a starting material or intermediate in the synthesis of more complex molecules with potential applications in various industries, including pharmaceuticals, agrochemicals, and materials science.
Check Digit Verification of cas no
The CAS Registry Mumber 5874-11-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,8,7 and 4 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 5874-11:
(6*5)+(5*8)+(4*7)+(3*4)+(2*1)+(1*1)=113
113 % 10 = 3
So 5874-11-3 is a valid CAS Registry Number.
5874-11-3Relevant articles and documents
EPR spectra and spin density distribution of O, S-dimethyl 4,4-dithioterephthalate radical anions
Voss, Juergen,Buddensiek, Dirk,Rosenboom, Jan Folkert
experimental part, p. 382 - 391 (2012/04/10)
The preparation of O-methyl S-trideuteromethyl 4,4-dithioterephthalate and S-methyl O-trideuteromethyl 4,4-dithioterephthalate is described. The EPR spectra of the corresponding radical anions are measured. Comparison with the spectrum of O,S-dimethyl 4,4
