129303-28-2 Usage
Description
(3aR,9aS)-4-[(4-chlorophenyl)carbonyl]-1,3,3a,4,9,9a-hexahydrothieno[3,4-b]quinoxaline 2,2-dioxide is a heterocyclic chemical compound with the molecular formula C17H18ClNO3S. It features a thienoquinoxaline core structure, with a 4-(4-chlorophenyl)carbonyl group attached to the ring system and a 2,2-dioxide substituent. This unique structure and composition may endow it with potential pharmaceutical applications, although further research is required to fully explore its uses and effects.
Uses
Used in Pharmaceutical Industry:
(3aR,9aS)-4-[(4-chlorophenyl)carbonyl]-1,3,3a,4,9,9a-hexahydrothieno[3,4-b]quinoxaline 2,2-dioxide is used as a potential pharmaceutical agent due to its distinctive structure and properties. The presence of the thienoquinoxaline core and the 4-(4-chlorophenyl)carbonyl group may contribute to its interaction with biological targets, offering possible therapeutic benefits. However, the specific applications and mechanisms of action need to be determined through additional studies and research.
Check Digit Verification of cas no
The CAS Registry Mumber 129303-28-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,9,3,0 and 3 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 129303-28:
(8*1)+(7*2)+(6*9)+(5*3)+(4*0)+(3*3)+(2*2)+(1*8)=112
112 % 10 = 2
So 129303-28-2 is a valid CAS Registry Number.
129303-28-2Relevant articles and documents
Thieno- and isothiazolo[3,4-b]quinoxalines: synthesis, structure and pharmacological study
Vierfond,Legendre,Martin,Rinjard,Miocque
, p. 251 - 255 (2007/10/02)
Thieno- and isothiazolo[3,4-b]quinoxalines have been prepared by annelation of quinoxaline. The stereochemistry of these molecules has been studied by 1H and 13C NMR. A preliminary biological study was performed for analgesic and anti-inflammatory activities. Among the studied compounds, 1,3,3a,4,9,9a-hexahydrothieno[3,4-b]quinoxaline 2,2-dioxide (1) shows potent anti-inflammatory activity in the carrageenin test.
