59878-63-6 Usage
Description
N-DESMETHYL ZOPICLONE, also known as a metabolite of Zopiclone, is an intermediate compound in the synthesis of N-DESMETHYL ZOPICLONE Hydrochloride. It is characterized by its white to off-white solid appearance.
Uses
Used in Pharmaceutical Industry:
N-DESMETHYL ZOPICLONE is used as an intermediate in the synthesis of N-DESMETHYL ZOPICLONE Hydrochloride (D296770) for its role in the production of medications that target sleep disorders and anxiety.
Used in Sleep Aid Applications:
N-DESMETHYL ZOPICLONE is used as a metabolite in the development of sleep aid medications, specifically for its potential role in improving sleep quality and duration.
Used in Anxiety Treatment:
N-DESMETHYL ZOPICLONE is used as a component in the formulation of anti-anxiety medications, potentially contributing to the relief of anxiety symptoms and promoting a sense of calm.
Check Digit Verification of cas no
The CAS Registry Mumber 59878-63-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,8,7 and 8 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 59878-63:
(7*5)+(6*9)+(5*8)+(4*7)+(3*8)+(2*6)+(1*3)=196
196 % 10 = 6
So 59878-63-6 is a valid CAS Registry Number.
InChI:InChI=1/C16H15ClN6O3/c17-10-1-2-11(21-9-10)23-14(24)12-13(20-4-3-19-12)15(23)26-16(25)22-7-5-18-6-8-22/h1-4,9,15,18H,5-8H2
59878-63-6Relevant articles and documents
Electrochemical oxidation of zopiclone
Tborsk, Jakub,vidrnoch, Martin,Kurka, Ondej,Borovcov, Lucie,Bedn, Petr,Bartk, Petr,Skopalov, Jana
, p. 53 - 60 (2016/01/09)
Electrochemical behaviour of zopiclone was investigated on glassy carbon electrode in static and rotation disc arrangement. Strong influence of kinetics and adsorption phenomena on the electrode processes was proved by voltammetric techniques. Controlled potential electrolysis in off-line and on-line combination with tandem mass spectrometry was employed for investigation of the products of electrochemical oxidation. N-Desmethyl zopiclone was identified and three other oxidation products formed by an introduction of one or two oxygen atom(s) to the molecule of zopiclone (including zopiclone N-oxide) were characterized. Based on mass spectrometric investigation of those products, piperazine moiety was proved as a target of electrochemical oxidation of zopiclone. Since N-desmethyl zopiclone and zopiclone N-oxide have been reported as products of enzymatic metabolism of the drug, the combination of electrochemistry with mass spectrometry may be considered as a reliable tool for simulation of some metabolic transformations. Graphical abstract: [Figure not available: see fulltext.]