160657-04-5 Usage
Uses
Used in Pharmaceutical Industry:
Pyrrolo[1,2-a]quinoxalin-4(5H)-one, 8-chlorois used as a potential pharmacological agent for its diverse biological activities. It has been studied for its potential as an anticancer, antifungal, and antibacterial agent.
Used in Anticancer Applications:
Pyrrolo[1,2-a]quinoxalin-4(5H)-one, 8-chlorois used as a potential anticancer agent. Further research is needed to fully understand its biological activities and potential therapeutic uses in treating various types of cancer.
Used in Antifungal Applications:
Pyrrolo[1,2-a]quinoxalin-4(5H)-one, 8-chlorois used as a potential antifungal agent. Its heterocyclic structure and 8-chloro substitution may contribute to its antifungal properties.
Used in Antibacterial Applications:
Pyrrolo[1,2-a]quinoxalin-4(5H)-one, 8-chlorois used as a potential antibacterial agent. Its unique structure and functional groups may provide antibacterial activity against various bacterial strains.
Check Digit Verification of cas no
The CAS Registry Mumber 160657-04-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,0,6,5 and 7 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 160657-04:
(8*1)+(7*6)+(6*0)+(5*6)+(4*5)+(3*7)+(2*0)+(1*4)=125
125 % 10 = 5
So 160657-04-5 is a valid CAS Registry Number.
160657-04-5Relevant academic research and scientific papers
Synthesis of pyrrole and indole quinoxalinone and oxazinone derivatives by intramolecular copper-catalyzed reactions
Vaillard, Victoria A.,Rossi, Roberto A.,Martin, Sandra E.
, p. 4927 - 4935 (2011/08/06)
Intramolecular N-arylation of pyrrole and indole carboxamides and carboxylates linked with a pendant haloarene by Cu-catalyzed reactions to synthesize pyrrole and indole quinoxalinone and oxazinone derivatives is reported. The ring closure reactions were carried out by conventional heating and MW irradiation. The use of conventional heating affords moderate to good yields of the quinoxalinone and oxazinone derivatives (34-72%), while by using MW heating the best results are obtained (41-99%). The Royal Society of Chemistry 2011.
