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thalicminine

Base Information
  • Chemical Name:thalicminine
  • CAS No.:16408-77-8
  • Molecular Formula:C20H15NO6
  • Molecular Weight:365.342
  • Hs Code.:
  • Mol file:16408-77-8.mol
thalicminine

Synonyms:Noraporphin-7-one,4,5,6,6a-tetradehydro-3,9,10-trimethoxy-1,2-(methylenedioxy)- (8CI);Thalicminine

Suppliers and Price of thalicminine
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
Total 4 raw suppliers
Chemical Property of thalicminine
Chemical Property:
  • Vapor Pressure:5.57E-15mmHg at 25°C 
  • Boiling Point:613.4°C at 760 mmHg 
  • Flash Point:324.7°C 
  • PSA:76.11000 
  • Density:1.43g/cm3 
  • LogP:3.20070 
Purity/Quality:

99% *data from raw suppliers

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

SDS file from LookChem

Useful:
  • Description The roots of Thalictrum minus contain this 10-oxoaporphine alkaloid which contains three methoxyl groups, a methylenedioxy group and a conjugated keto group. Prolonged reduction with Zn dust in AcOH-H2S04 gives the hexahydro derivative, m.p. 180-2°C which has an ultraviolet spectrum in EtOH showing absorption maxima at 218,280 and 302 II1J1. The alkaloid is formed by the oxidation of Thalicmine (q.v.) with KMn04 in Me2CO or chromic acid in pyridine.
Technology Process of thalicminine

There total 1 articles about thalicminine 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:

Guidance literature:
O-Methyl-cassyfilin, CrO3-Oxid.;
DOI:10.1021/jo01270a059
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