65514-72-9 Usage
Type of Compound
Piperazine derivative
Structural Features
Contains a benzoyl group
Chlorine and nitro substituents on the phenyl ring
Potential Applications
Antidepressant medication
Antipsychotic medication
Treatment for Parkinson's disease and other neurological disorders
Receptor Interactions
Exhibits high affinity for specific serotonin and dopamine receptor subtypes
Central Nervous System Effects
Suggests potential therapeutic effects on the central nervous system
Research Status
Further research needed to fully understand the potential pharmacological effects and safety profile of the compound
Check Digit Verification of cas no
The CAS Registry Mumber 65514-72-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,5,1 and 4 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 65514-72:
(7*6)+(6*5)+(5*5)+(4*1)+(3*4)+(2*7)+(1*2)=129
129 % 10 = 9
So 65514-72-9 is a valid CAS Registry Number.
InChI:InChI=1/C18H19ClN4O3/c1-21-8-10-22(11-9-21)18(24)14-4-2-3-5-15(14)20-16-7-6-13(19)12-17(16)23(25)26/h2-7,12,20H,8-11H2,1H3
65514-72-9Relevant articles and documents
Direct Reductive Cyclocondensation of the Nitro Group with the Amido Group: Key Role of the Iminophosphorane Intermediate in the Synthesis of 1,4-Dibenzodiazepine Derivatives
Tryniszewski, Micha?,Bujok, Robert,Cmoch, Piotr,Gańczarczyk, Roman,Kulszewicz-Bajer, Irena,Wróbel, Zbigniew
, p. 2277 - 2286 (2019/05/16)
A class of dialkylamino-substituted dibenzodiazepines and their hetero analogues was synthesized by the intramolecular aza-Wittig condensation of the amido group with iminophosphoranes. The one-pot, two-step procedure includes reductive synthesis of the intermediate iminophosphoranes from the corresponding nitroamides and tributylphosphine.
