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1,6-anhydro cellopentaose

Base Information
  • Chemical Name:1,6-anhydro cellopentaose
  • CAS No.:122274-98-0
  • Molecular Formula:C30H50O25
  • Molecular Weight:810.712
  • Hs Code.:
1,6-anhydro cellopentaose

Synonyms:1,6-anhydro cellopentaose

Suppliers and Price of 1,6-anhydro cellopentaose
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
  • 1,6-Anhydro-b-D-cellopentose
  • 1mg
  • $ 479.00
  • Biosynth Carbosynth
  • 1,6-Anhydro-b-D-cellopentose
  • 2 mg
  • $ 300.00
  • Biosynth Carbosynth
  • 1,6-Anhydro-b-D-cellopentose
  • 1 mg
  • $ 163.00
  • Biosynth Carbosynth
  • 1,6-Anhydro-b-D-cellopentose
  • 5 mg
  • $ 680.00
  • Biosynth Carbosynth
  • 1,6-Anhydro-b-D-cellopentose
  • 20 mg
  • $ 2360.00
  • Biosynth Carbosynth
  • 1,6-Anhydro-b-D-cellopentose
  • 10 mg
  • $ 1240.00
  • Apolloscientific
  • 1,6-Anhydro-beta-D-cellopentaose 98%min
  • 5mg
  • $ 1233.00
  • Apolloscientific
  • 1,6-Anhydro-beta-D-cellopentaose 98%min
  • 2mg
  • $ 566.00
  • Apolloscientific
  • 1,6-Anhydro-beta-D-cellopentaose 98%min
  • 1mg
  • $ 341.00
Total 2 raw suppliers
Chemical Property of 1,6-anhydro cellopentaose
Chemical Property:
Purity/Quality:

95% *data from raw suppliers

1,6-Anhydro-b-D-cellopentose *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
Technology Process of 1,6-anhydro cellopentaose

There total 1 articles about 1,6-anhydro cellopentaose 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 2-chloro-1,3-dimethylimidazolinium chloride; triethylamine; In water; at 0 ℃; for 0.25h;
DOI:10.1016/j.tetlet.2009.02.171
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