130064-16-3 Usage
Derivative of quinoxaline
Quinoxaline is a heterocyclic organic compound with a ring structure containing two nitrogen atoms. 2,3-Dimethoxy-6,7-dimethylquinoxaline is a modified version of this compound.
Methoxy and methyl groups
The compound has two methoxy (CH3O) groups and two methyl (CH3) groups attached to the quinoxaline ring, which influence its chemical properties and reactivity.
Organic synthesis building block
2,3-Dimethoxy-6,7-dimethylquinoxaline is used in organic synthesis as a starting material for constructing more complex compounds.
Potential applications
The compound may have potential uses in the pharmaceutical and agricultural industries, depending on the context of its application. Its specific uses and properties may vary in different settings.
Check Digit Verification of cas no
The CAS Registry Mumber 130064-16-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,0,0,6 and 4 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 130064-16:
(8*1)+(7*3)+(6*0)+(5*0)+(4*6)+(3*4)+(2*1)+(1*6)=73
73 % 10 = 3
So 130064-16-3 is a valid CAS Registry Number.
130064-16-3Relevant articles and documents
1,4-Dihydro-2,3-quinoxalinediones as potential flavin metabolites and excitatory amino acid receptor ligands. Part 1: Synthesis and pharmacological evaluation of the benzylic oxidation series of 1,4-dihydro-6,7-dimethyl-2,3- quinoxalinedione
Bhat, Ajita,Chang, Hui-Min,Wallace, Lane J.,Weinstein, David M.,Shams, Gamal,Garris, Cynthia C.,Hill, Ronald A.
, p. 271 - 282 (2007/10/03)
A series of five 6,7-disubstituted 1,4-dihydro-2,3-quinoxalinediones was prepared, two of which are known microbial flavin metabolites and three of which are potential flavin metabolites. Four of the five compounds inhibited specific binding of [3H]-amino-3-hydroxy-5-methyl-4-isoxazolepropanoic acid ([3H]AMPA), [3H]kainic acid, and [3H]6-cyano-1,4-dihydro-7-nitro-2,3- quinoxalinedione ([3H]CNQX) in rat brain homogenate fractions, with IC50 values in the low micromolar range (the fifth compound competed only with [3H]CNQX). Two of the compounds were moderately potent AMPA antagonists in an in vitro functional test.
