156243-39-9 Usage
Explanation
The compound is composed of 13 carbon atoms, 14 hydrogen atoms, and 4 nitrogen atoms.
Explanation
It contains a fused imidazole and quinoxaline ring system, which are both heterocyclic in nature.
Explanation
The imidazole ring is connected to the quinoxaline ring, forming a fused ring system.
Explanation
The compound has an amino group (-NH2) attached to the second carbon atom of the imidazole ring.
Explanation
The imidazole ring has three methyl groups (-CH3) attached at the 1st, 7th, and 9th positions.
Explanation
The compound belongs to the imidazo[4,5-g]quinoxalin-2-amine family of compounds.
Explanation
Due to its unique structure and properties, the compound has potential applications in the fields of medicinal chemistry and drug development.
Explanation
The specific arrangement of the fused rings and functional groups in the compound may contribute to its potential for biological activity and therapeutic use.
Chemical structure
Heterocyclic compound
Imidazole ring
Fused to a quinoxaline ring
Amino group
Attached to the second carbon
Methyl groups
Three methyl groups at positions 1, 7, and 9
Family
Imidazo[4,5-g]quinoxalin-2-amine
Applications
Medicinal chemistry and drug development
Unique structure
Potential for biological activity
Check Digit Verification of cas no
The CAS Registry Mumber 156243-39-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,6,2,4 and 3 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 156243-39:
(8*1)+(7*5)+(6*6)+(5*2)+(4*4)+(3*3)+(2*3)+(1*9)=129
129 % 10 = 9
So 156243-39-9 is a valid CAS Registry Number.
156243-39-9Relevant academic research and scientific papers
Synthesis and mutagenicity of a new mutagen, 2-amino-1,7,9- trimethylimidazo-[4,5-g]quinoxaline, and its analog
Achiwa,Shiozawa,Nukaya,Terao
, p. 408 - 409 (2007/10/02)
A new mutagen, 2-amino-1,7,9-trimethylimidazo-[4,5-g]quinoxaline (1), isolated from beef extract, was synthesized from 3-fluoro-2-methylaniline via an intermediate, 2,8-dimethyl-7-methylaminoquinoxaline (7a). Its 2- methylanalog (2) was also synthesized from the same intermediate. The synthetic 1 showed the same mutagenic activity as the isolated mutagen. However, 2 was non-mutagenic.
