76672-25-8 Usage
Uses
Used in Pharmaceutical Synthesis:
2,6-Dichloro-3-phenylquinoxaline is used as a key intermediate in the synthesis of various pharmaceutical compounds. Its unique chemical structure allows for the development of new drugs with potential therapeutic benefits.
Used in Agrochemical Synthesis:
In the agrochemical industry, 2,6-Dichloro-3-phenylquinoxaline is utilized as a precursor for the production of pesticides and other agrochemicals. Its incorporation into these products can enhance their effectiveness in controlling pests and diseases in agriculture.
Used in Antibacterial Applications:
2,6-Dichloro-3-phenylquinoxaline is used as an antibacterial agent due to its ability to inhibit the growth of certain bacteria. This property makes it a potential candidate for the development of new antibiotics to combat bacterial infections.
Used in Antifungal Applications:
2,6-Dichloro-3-phenylquinoxaline is also used as an antifungal agent, demonstrating its potential to treat fungal infections by inhibiting the growth of fungi.
Used in Anti-inflammatory Applications:
2,6-Dichloro-3-phenylquinoxaline exhibits anti-inflammatory properties, making it a candidate for the development of new therapeutic agents to treat inflammatory conditions.
Used in Therapeutic Agent Development:
Owing to its diverse biological activities, 2,6-Dichloro-3-phenylquinoxaline is being studied for its potential use in the development of new therapeutic agents for the treatment of various diseases, pending further investigation into its safety and efficacy.
Check Digit Verification of cas no
The CAS Registry Mumber 76672-25-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,6,7 and 2 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 76672-25:
(7*7)+(6*6)+(5*6)+(4*7)+(3*2)+(2*2)+(1*5)=158
158 % 10 = 8
So 76672-25-8 is a valid CAS Registry Number.
76672-25-8Relevant academic research and scientific papers
Quinoxaline chemistry. Part 6. Synthesis and evaluation of antiulcer and gastroprotective activity of 2-[arylmethylmercapto-,arylmethylsulfinyl-,piperazinyl-3-R-substituted ]quinoxalines
Piras,Loriga,Paglietti,Demontis,Varoni,Fattaccio,Anania
, p. 569 - 577 (2007/10/03)
Thirty compounds possessing quinoxaline structure bearing either substituted arylmethylmercapto-, arylmethylsulfinyl group or a piperazinyl moiety in position 2 were prepared in order to evaluate an antiulcer and gastroprotective activity in rat pylorus ligature, in comparison with omeprazole and ranitidine at the dose of 100 mg/kg after oral administration. Among the compounds of the first group one third showed a moderate activity being about half potent as omeprazole whereas in the second group compound 5b exhibited an activity superior to that of ranitidine accompanied with the lowest incidence of lesions and mortality and another compound (5i) was equiactive as ranitidine.
