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S(+)-Mianserin

Base Information
  • Chemical Name:S(+)-Mianserin
  • CAS No.:51152-88-6
  • Molecular Formula:C18H20N2
  • Molecular Weight:264.37
  • Hs Code.:
  • Mol file:51152-88-6.mol
S(+)-Mianserin

Synonyms:Dibenzo[c,f]pyrazino[1,2-a]azepine,1,2,3,4,10,14b-hexahydro-2-methyl-, (S)-; (+)-(S)-Mianserin; (+)-Mianserin;(S)-Mianserin; Mianserin, (+)-; S(+)-Mianserin

Suppliers and Price of S(+)-Mianserin
Supply Marketing:
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
  • TRC
  • (S)-(+)-Mianserin
  • 25mg
  • $ 395.00
  • American Custom Chemicals Corporation
  • S(+)-MIANSERIN 95.00%
  • 5MG
  • $ 502.46
Total 11 raw suppliers
Chemical Property of S(+)-Mianserin
Chemical Property:
  • Vapor Pressure:5.65E-07mmHg at 25°C 
  • Boiling Point:411.3°Cat760mmHg 
  • Flash Point:186.1°C 
  • PSA:6.48000 
  • Density:1.18g/cm3 
  • LogP:3.08680 
Purity/Quality:

99% *data from raw suppliers

(S)-(+)-Mianserin *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Uses (S)-(+)-Mianserin is serotonin receptor antagonist. Antidepressant.
Technology Process of S(+)-Mianserin

There total 12 articles about S(+)-Mianserin 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:
With potassium carbonate; In tetrahydrofuran; at 24 - 25 ℃; for 2.5h;
DOI:10.3762/bjoc.11.164
Guidance literature:
Title compound not separated from byproducts;
Guidance literature:
(14bR)-2-[(1'S)-1'-phenylethyl]-1,2,3,4,10,14b-hexahydrodibenzo[c,f]pyrazino[1,2-a]azepine; With hydrogenchloride; hydrogen; palladium on activated charcoal; In ethanol; water; for 3h; atmospheric pressure;
formaldehyd; In ethanol; water; at 10 ℃;
With sodium tetrahydroborate; In ethanol; water; Title compound not separated from byproducts;
DOI:10.1016/S0957-4166(03)00582-2
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