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Sophoridine

Base Information
  • Chemical Name:Sophoridine
  • CAS No.:83148-91-8
  • Molecular Formula:C15H24N2O
  • Molecular Weight:248.368
  • Hs Code.:
Sophoridine

Synonyms:(+)-Sophoridine;d-Sophoridine;

Suppliers and Price of Sophoridine
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
  • Usbiological
  • Sophoridine
  • 20mg
  • $ 320.00
  • Medical Isotopes, Inc.
  • (+)-Sophoridine
  • 10 mg
  • $ 650.00
  • DC Chemicals
  • Sophoridine >98%
  • 20 mg
  • $ 280.00
  • Biorbyt Ltd
  • Sophoridine
  • 100 mg
  • $ 408.00
  • Biorbyt Ltd
  • Sophoridine
  • 20 mg
  • $ 238.00
  • ApexBio Technology
  • Sophoridine
  • 20mg
  • $ 50.00
Total 35 raw suppliers
Chemical Property of Sophoridine
Chemical Property:
  • Boiling Point:396.7 °C at 760 mmHg 
  • PKA:9.47±0.20(Predicted) 
  • Flash Point:172.7 °C 
  • PSA:23.55000 
  • Density:1.16 g/cm3 
  • LogP:1.74750 
  • Solubility.:Chloroform (Slightly), Methanol (Slightly), Water (Slightly) 
Purity/Quality:

99% *data from raw suppliers

Sophoridine *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Description One of a number of minor alkaloids isolated from Leontice albertii Rgl., this base crystallizes from petroleum ether as colourless prisms. It is dextrorotatory having a specific rotation of [α]D + 59.3° (c 1.3, EtOH) and yields a crystalline methiodide, m.p. 249°C. The structure has been assigned on the basis of chemical analysis and spectroscopic determinations.
  • Uses (+)-Sophoridine acts as an anti-inflammatory agent in vitro and in vivo. Anticancer agent, with a promising anti-tumor effect and lower toxicity.
Technology Process of Sophoridine

There total 2 articles about Sophoridine 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:
C15H26N2O2; With thionyl chloride; In 1,2-dichloro-ethane; at 0 - 70 ℃;
With 4-(2-hydroxyethoxy)-3-(phenylsulfonyl)-1,2,5-oxadiazole 2-N-oxide; dmap; dicyclohexyl-carbodiimide; In 1,2-dichloro-ethane;
With di-tert-butyl oxalate; sodium hydroxide; In water; 1,2-dichloro-ethane; tert-butyl alcohol;
DOI:10.1016/j.cclet.2009.11.033
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