63376-31-8 Usage
Molecular structure
The compound has a triazole ring fused to a tetrone ring, with two 4-chlorophenyl substituents on the 2 and 6 positions.
Heterocyclic compound
It belongs to the group of triazoles, which are known for their wide range of biological activities.
Biological activities
Triazoles exhibit antifungal, antiviral, and anticancer properties.
Potential use
The presence of the tetrone ring and chlorophenyl groups suggests that 1H,5H-[1,2,4]Triazolo[1,2-a][1,2,4]triazole-1,3,5,7(2H,6H)-tetrone,
2,6-bis(4-chlorophenyl)- may have potential use in medicinal chemistry for developing new drugs with targeted biological activities.
Further research needed
More research and testing are required to fully understand the properties and potential applications of 1H,5H-[1,2,4]Triazolo[1,2-a][1,2,4]triazole-1,3,5,7(2H,6H)-tetrone,
2,6-bis(4-chlorophenyl)-.
Check Digit Verification of cas no
The CAS Registry Mumber 63376-31-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,3,7 and 6 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 63376-31:
(7*6)+(6*3)+(5*3)+(4*7)+(3*6)+(2*3)+(1*1)=128
128 % 10 = 8
So 63376-31-8 is a valid CAS Registry Number.
63376-31-8Relevant academic research and scientific papers
Reaction of Diazoalkanes with 4-Substituted 1,2,4-Triazole-3,5(4H)-diones
Izydore, Robert A.,Chapman, John J.,Mitchell, John A.,Cummings, Robert,Jones, George T.
, p. 1415 - 1422 (2007/10/02)
Diazoacetic esters reacted with 4-substituted 1,2,4-triazole-3,5(4H)-diones (2) to give one-to-one adducts.Molecular weight determination, high-performance-liquid chromatography, and 2D n.m.r. spectroscopy showed that the adducts are monomers that associate in solution.The monomers are most likely 1,3,5-triazabicyclohexane-2,4-diones.The adducts were thermally isomerized to 3,6-disubstituted 1,3,5-triazine-2,4(1H,3H)-diones.Diphenyldiazomethane reacted with (2) to yield an azomethine imine, which underwent thermal dimerization followed by rearrangement.
