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torularhodin

Base Information Edit
  • Chemical Name:torularhodin
  • CAS No.:514-92-1
  • Molecular Formula:C40H52O2
  • Molecular Weight:564.852
  • Hs Code.:
  • Mol file:514-92-1.mol
torularhodin

Synonyms:

Suppliers and Price of torularhodin
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
Total 15 raw suppliers
Chemical Property of torularhodin Edit
Chemical Property:
  • Vapor Pressure:1.57E-23mmHg at 25°C 
  • Boiling Point:733.4°Cat760mmHg 
  • Flash Point:559.8°C 
  • Density:0.981g/cm3 
Purity/Quality:

99% *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
Technology Process of torularhodin

There total 6 articles about torularhodin 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 hydroxide; In methanol; for 2h; Reflux;
DOI:10.1016/j.tet.2012.10.041
Guidance literature:
Multi-step reaction with 3 steps
1.1: sodium methylate / methanol / 24 h / Reflux
1.2: 2 h
2.1: sodium methylate / methanol; tetrahydrofuran / 48 h
3.1: potassium hydroxide / methanol / 2 h / Reflux
With sodium methylate; potassium hydroxide; In tetrahydrofuran; methanol; 2.1: |Wittig Olefination;
DOI:10.1016/j.tet.2012.10.041
Guidance literature:
Multi-step reaction with 2 steps
1: sodium methylate / methanol; tetrahydrofuran / 48 h
2: potassium hydroxide / methanol / 2 h / Reflux
With sodium methylate; potassium hydroxide; In tetrahydrofuran; methanol; 1: |Wittig Olefination;
DOI:10.1016/j.tet.2012.10.041
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