7092-76-4 Usage
Molecular Weight
132.16 g/mol
Class
1,5-Benzodiazepine derivative
Structural Relation
Related to benzodiazepine drugs
Central Nervous System (CNS) Effects
Depressant
Pharmacological Effects
Sedative, hypnotic, anxiolytic, anticonvulsant, and muscle-relaxant properties
Therapeutic Applications
Treatment of anxiety, insomnia, and seizure disorders
Potential for Abuse
Known to have a potential for abuse and dependence
Legal Status
Categorized as a controlled substance in many countries
Check Digit Verification of cas no
The CAS Registry Mumber 7092-76-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,0,9 and 2 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 7092-76:
(6*7)+(5*0)+(4*9)+(3*2)+(2*7)+(1*6)=104
104 % 10 = 4
So 7092-76-4 is a valid CAS Registry Number.
7092-76-4Relevant articles and documents
DIAZABICYCLOALKANES WITH NITROGEN ATOMS IN THE NODAL POSITIONS. 10. INTRAMOLECULAR CYCLIZATION OF β-BROMOETHYL-AND γ-BROMOPROPYL-N,N'-ALKYLENE-o-PHENYLENEDIAMINES
Gall', A. A.,Shishkin, G. V.
, p. 553 - 558 (1983)
The overall scheme of the intramolecular cyclization of bromoalkyl derivatives of N,N'-alkylene-o-phenylenediamines in HBr was established, and the rates of the individual steps of this complex process were estimated.It is shown that N-(β-bromoethyl)-N,N'-trimethylene-o-phenylenediamine undergoes virtually irreversible cyclization at a high rate to give benzo-1,5-diazabicyclo-nonene in significant yield, while the cyclization of N-(γ-bromopropyl)-1,2,3,4-tetrahydroquinoxaline proceeds at commensurable rates via two pathways, viz., C- and N-alkylation.This makes it impossible to use the latter reaction to obtain benzo-1,5-diazabicyclononene in high yield.
