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Pyrrolidine, 1-[3-(butylthio)-1-thioxopropyl]- (9CI)

Base Information
  • Chemical Name:Pyrrolidine, 1-[3-(butylthio)-1-thioxopropyl]- (9CI)
  • CAS No.:73199-97-0
  • Molecular Formula:C11H21NS2
  • Molecular Weight:231.426
  • Hs Code.:
  • Mol file:73199-97-0.mol
Pyrrolidine,  1-[3-(butylthio)-1-thioxopropyl]-  (9CI)

Synonyms:Pyrrolidine,1-[3-(butylthio)-1-thioxopropyl]- (9CI)

Suppliers and Price of Pyrrolidine, 1-[3-(butylthio)-1-thioxopropyl]- (9CI)
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 2 raw suppliers
Chemical Property of Pyrrolidine, 1-[3-(butylthio)-1-thioxopropyl]- (9CI)
Chemical Property:
  • PSA:60.63000 
  • LogP:3.27090 
Purity/Quality:

98% *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
Technology Process of Pyrrolidine, 1-[3-(butylthio)-1-thioxopropyl]- (9CI)

There total 2 articles about Pyrrolidine, 1-[3-(butylthio)-1-thioxopropyl]- (9CI) 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 diphosphorus pentasulfide; In xylene; for 1h; Heating;
DOI:10.1021/jo01298a022
Guidance literature:
Multi-step reaction with 2 steps
1: 1.) thionyl chloride, dimethylformamide / 1.) room temperature, 16 h, 2.) dichloromethane, added over 30 min to ice-cold solution, then room temperature, 1 h
2: 63 percent / phosphorus pentasulfide / xylene / 1 h / Heating
With diphosphorus pentasulfide; thionyl chloride; N,N-dimethyl-formamide; In xylene;
DOI:10.1021/jo01298a022
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