93417-16-4 Usage
Chemical structure
1H-Imidazo[4,5-f]quinoxaline core with a 4-chlorophenyl group attached at the 2-position
Classification
Heterocyclic compound
Target enzyme
Phosphodiesterase 10A (PDE10A)
Function
Potent and selective inhibitor of PDE10A, which regulates levels of dopamine and adenosine in the central nervous system
Therapeutic applications
Treatment of neurological and psychiatric disorders (e.g. schizophrenia, Huntington's disease, Parkinson's disease), movement disorders, and cognitive impairments
Potential use
Management of various central nervous system-related conditions
Check Digit Verification of cas no
The CAS Registry Mumber 93417-16-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,4,1 and 7 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 93417-16:
(7*9)+(6*3)+(5*4)+(4*1)+(3*7)+(2*1)+(1*6)=134
134 % 10 = 4
So 93417-16-4 is a valid CAS Registry Number.
93417-16-4Relevant academic research and scientific papers
Synthesis of 2-Sustituted 1H-Imidazoquinoxalines
Kishan Rao, S.,Pandu Ranga Reddy, A.,Veerangaiah, V.
, p. 960 - 961 (2007/10/02)
Condensation of 5,6-diaminoquinoxaline (I) with aliphatic and aromatic acids under catalytic and thermal conditions yields the corresponding 2-alkyl/aryl-1H-imidazoquinoxalines (III).
Studies on Formation of Imidazoquinoxalines from Quinoxaline-5,6-diamine and Aromatic Aldehydes
Rao, S. Kishan,Veeranagaiah, V.
, p. 525 - 528 (2007/10/02)
Condensation of quinoxaline-5,6-diamine (I) with aromatic aldehydes in acetic acid yields 2-aryl-1(or 3)H-imidazoquinoxalines (II), 2-aryl-3-arylmethyl-3H-imidazoquinoxalines (III), 2-aryl-1-arylmethyl-1H-imidazoquinoxalines (IV) and
