86663-66-3 Usage
Chemical class
Pyridoquinoxalines
Explanation
123DBQ belongs to a class of bicyclic heterocyclic compounds with a pyridine ring fused to a quinoxaline ring.
Explanation
123DBQ has been studied for its interactions with different receptors, which could lead to therapeutic applications.
Explanation
123DBQ has demonstrated the ability to alleviate pain in early-stage research.
Explanation
123DBQ has shown promise in treating symptoms of psychosis in early-stage research.
Explanation
123DBQ has demonstrated the ability to enhance cognitive performance in early-stage research.
Explanation
123DBQ has been explored for its potential to alleviate symptoms and improve the quality of life for patients with neurological disorders.
Explanation
More research is required to fully comprehend the effects, safety, and potential uses of 123DBQ in various therapeutic contexts.
Pharmacological activities
Potential as a ligand for various receptors
Analgesic potential
Preclinical studies have shown its potential as a pain reliever
Antipsychotic potential
Preclinical studies have shown its potential as an antipsychotic agent
Cognitive enhancer potential
Preclinical studies have shown its potential to improve cognitive function
Treatment of neurological disorders
Investigated for use in treating conditions like Parkinson's disease and mood disorders
Further research needed
Limited understanding of its pharmacological properties and clinical applications
Check Digit Verification of cas no
The CAS Registry Mumber 86663-66-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,6,6 and 3 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 86663-66:
(7*8)+(6*6)+(5*6)+(4*6)+(3*3)+(2*6)+(1*6)=173
173 % 10 = 3
So 86663-66-3 is a valid CAS Registry Number.
86663-66-3Relevant articles and documents
DIAZABICYCLOALKANES WITH NITROGEN ATOMS IN THE NODAL POSITIONS. 9. INTRAMOLECULAR CYCLIZATION OF N-(γ-BROMOPROPYL)-TETRAHYDROQUINOXALINES AND BEHAVIOR OF BENZO-1,5-DIAZABICYCLONONENE IN HYDROBROMIC ACID
Gall', A. A.,Shishkin, G. V.
, p. 549 - 553 (1983)
The introduction of an N,N'-trimethylene bridge in the tetrahydroquinoxaline molecule is complicated by cyclization of γ-bromopropyl derivatives of tetrahydroquinoxaline at the carbon atom of the aromatic ring.The reaction of N-R-tetrahydroquinoxalines (R = H, COCH3) which 1,3-dibromopropane leads to products of cyclization at the aromatic ring (1,2,3,5,6,8,9,10-octahydropyrazinophenanthroline and N-acetyl-1,2,6,7-tetrahydro-3H,5H-pyridoquinoxaline) and to an N-alkylation product .Benzo-1,5-diazabicyclononene is formed in only trace amounts in the cyclization of N-(γ-bromopropyl) tetrahydroquinoxaline and upon heating in HBr can be isomerized with migration of the trimethylene bridge to the aromatic ring.
