Zopiclone N-oxide

Base Information

• Chemical Name: Zopiclone N-oxide
• CAS No.: 43200-96-0
• Molecular Formula: C₁₇H₁₇ClN₆O₄
• Molecular Weight: 404.813
• Hs Code.: 2933790002
• European Community (EC) Number: 641-896-9
• UNII: 0XXQ8C2EK4
• DSSTox Substance ID: DTXSID20962959
• Nikkaji Number: J528.451A
• Wikidata: Q27237324
• Mol file: 43200-96-0.mol

Synonyms:6-(5-chloro-2-pyridyl)-7-((4-oxo-4-methyl-1-piperazinyl)carbonyloxy)-6,7-dihydro(5H)pyrrolo(3,4-b)pyrazin-5-one;N-oxide-zopiclone;N-oxidezopiclone;OXZOP;zopiclone N-oxide

Chemical Property of Zopiclone N-oxide

Chemical Property:

• Melting Point: >140oC (dec.)
• PKA: 4.92±0.20(Predicted)
• Flash Point: 9℃
• PSA: 117.95000
• LogP: 1.54230
• Storage Temp.: -20°C Freezer
• Solubility.: Chloroform (Slightly, Heated), DMSO (Slightly), Methanol (Slightly, Heated, Soni
• XLogP3: -0.1
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 7
• Rotatable Bond Count: 3
• Exact Mass: 404.0999807
• Heavy Atom Count: 28
• Complexity: 617

Purity/Quality:

98%,99%, ^*data from raw suppliers

Zopiclone N-Oxide ^*data from reagent suppliers

Safty Information:

• Hazard Codes: F,T
• Statements: 11-23/24/25-39/23/24/25
• Safety Statements: 7-16-36/37-45

MSDS Files:

Useful:

• Canonical SMILES: C[N+]1(CCN(CC1)C(=O)OC2C3=NC=CN=C3C(=O)N2C4=NC=C(C=C4)Cl)[O-]
• Uses: A metabolite of Zopiclone Eszopiclone impurity A.

Technology Process of Zopiclone N-oxide

There total 1 articles about Zopiclone N-oxide which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

→ Zopiclone N-oxide (43200-96-0)

Guidance literature:

6-(5-Chloro-2-pyridyl)-(4-methyl-1-piperazinyl)-5-carbonyloxy-7-oxo-5,6-dihydropyrrolo<3,4-b>pyrazin in CHCl3, p-Nitroperbenzoesaeure;