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10-[3-(dimethylamino)propyl]-2-nitrodibenz[b,f][1,4]oxazepin-11(10H)-one monohydrochloride

Base Information Edit
  • Chemical Name:10-[3-(dimethylamino)propyl]-2-nitrodibenz[b,f][1,4]oxazepin-11(10H)-one monohydrochloride
  • CAS No.:16398-39-3
  • Molecular Formula:C18H19 N3 O4 . Cl H
  • Molecular Weight:377.827
  • Hs Code.:
  • Mol file:16398-39-3.mol
10-[3-(dimethylamino)propyl]-2-nitrodibenz[b,f][1,4]oxazepin-11(10H)-one monohydrochloride

Synonyms:Dibenz[b,f][1,4]oxazepin-11(10H)-one,10-[3-(dimethylamino)propyl]-2-nitro-, monohydrochloride (8CI,9CI); CIBA2330Go; Nitroxazepine; Sintamil

Suppliers and Price of 10-[3-(dimethylamino)propyl]-2-nitrodibenz[b,f][1,4]oxazepin-11(10H)-one monohydrochloride
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
Total 3 raw suppliers
Chemical Property of 10-[3-(dimethylamino)propyl]-2-nitrodibenz[b,f][1,4]oxazepin-11(10H)-one monohydrochloride Edit
Chemical Property:
  • Vapor Pressure:1.09E-10mmHg at 25°C 
  • Melting Point:227-229 °C(Solv: ethanol (64-17-5); ethyl ether (60-29-7)) 
  • Boiling Point:514.3°Cat760mmHg 
  • Flash Point:264.8°C 
  • PSA:78.60000 
  • Density:g/cm3 
  • LogP:3.88720 
Purity/Quality:

99% *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Uses Nitroxazepine is an impurity of Amoxapine (A634230), which is an antidepressant.
Technology Process of 10-[3-(dimethylamino)propyl]-2-nitrodibenz[b,f][1,4]oxazepin-11(10H)-one monohydrochloride

There total 1 articles about 10-[3-(dimethylamino)propyl]-2-nitrodibenz[b,f][1,4]oxazepin-11(10H)-one monohydrochloride 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:
Guidance literature:
Oxazepin I,Me2N-(CH2)3Cl*HCl II;
Guidance literature:
Multi-step reaction with 3 steps
1: xylene / 7 h / Heating
2: HBr / acetic acid
3: benzene
With hydrogen bromide; In acetic acid; xylene; benzene;
Guidance literature:
Multi-step reaction with 2 steps
1: ClCO2Et / xylene / 7 h / Heating
2: dimethylformamide / 16 h / 110 °C
With chloroformic acid ethyl ester; In N,N-dimethyl-formamide; xylene;
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