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8-HYDROXY MIRTAZAPINE

Base Information Edit
  • Chemical Name:8-HYDROXY MIRTAZAPINE
  • CAS No.:102335-57-9
  • Molecular Formula:C17H19N3O
  • Molecular Weight:281.357
  • Hs Code.:
  • Mol file:102335-57-9.mol
8-HYDROXY MIRTAZAPINE

Synonyms:8-Hydroxy-6-azamianserin;8-Hydroxymirtazapine

Suppliers and Price of 8-HYDROXY MIRTAZAPINE
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
  • Usbiological
  • 8-Hydroxy Mirtazapine
  • 1mg
  • $ 496.00
  • Usbiological
  • 8-Hydroxy Mirtazapine
  • 1mg
  • $ 446.00
  • Usbiological
  • 8-Hydroxy Mirtazapine
  • 1mg
  • $ 446.00
  • TRC
  • 8-HydroxyMirtazapine
  • 5mg
  • $ 175.00
  • American Custom Chemicals Corporation
  • 8-HYDROXY MIRTAZAPINE 95.00%
  • 10MG
  • $ 1904.02
  • American Custom Chemicals Corporation
  • 8-HYDROXY MIRTAZAPINE 95.00%
  • 1MG
  • $ 715.52
Total 8 raw suppliers
Chemical Property of 8-HYDROXY MIRTAZAPINE Edit
Chemical Property:
  • Vapor Pressure:0mmHg at 25°C 
  • Melting Point:>242°C (dec.) 
  • Boiling Point:559.604°C at 760 mmHg 
  • Flash Point:292.238°C 
  • PSA:39.60000 
  • Density:1.318g/cm3 
  • LogP:2.18740 
  • Storage Temp.:Refrigerator 
  • Solubility.:DMSO (Slightly), Methanol (Slightly, Sonicated) 
Purity/Quality:

98%Min *data from raw suppliers

8-Hydroxy Mirtazapine *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Uses 8-Hydroxy Mirtazapine is used in the synthesis of Mirtazapine (M365000) metabolite. Labelled metabolite of Mirtazapine (M365000). Labelled analog of the main metabolite of Mirtazapine (M365000).
Technology Process of 8-HYDROXY MIRTAZAPINE

There total 2 articles about 8-HYDROXY MIRTAZAPINE 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:
Multi-step reaction with 2 steps
1: 80 percent / bromine / acetic acid / 4 h / Ambient temperature
2: 1) BuLi, 2) nitrobenzene / 1) THF, hexane, -60 deg C, 45 mini580, 2) THF, hexane, -196 to -60 deg C and 3.5 h at -60 deg C
With n-butyllithium; bromine; nitrobenzene; In acetic acid;
DOI:10.1002/recl.19851041004
Guidance literature:
With n-butyllithium; nitrobenzene; Yield given. Multistep reaction; 1) THF, hexane, -60 deg C, 45 mini580, 2) THF, hexane, -196 to -60 deg C and 3.5 h at -60 deg C;
DOI:10.1002/recl.19851041004
Refernces Edit
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