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1,2,3-Tri-O-benzoyl-α-L-fucopyranose, Trichloroacetimidate

Base Information
  • Chemical Name:1,2,3-Tri-O-benzoyl-α-L-fucopyranose, Trichloroacetimidate
  • CAS No.:180476-30-6
  • Molecular Formula:C29H24Cl3NO8
  • Molecular Weight:620.87
  • Hs Code.:
  • Mol file:180476-30-6.mol
1,2,3-Tri-O-benzoyl-α-L-fucopyranose, Trichloroacetimidate

Synonyms:1,2,3-Tri-O-benzoyl-α-L-fucopyranose, Trichloroacetimidate;6-Deoxy-α-L-galactopyranose 2,3,4-Tribenzoate 1-(2,2,2-TrichloroethaniMidate);2,3,4-Tri-O-benzoyl-α-L-fucopyranose, TrichloroacetiMidate

Suppliers and Price of 1,2,3-Tri-O-benzoyl-α-L-fucopyranose, Trichloroacetimidate
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
  • TRC
  • 1,2,3-Tri-O-benzoyl-α-L-fucopyranose,Trichloroacetimidate
  • 100mg
  • $ 140.00
  • Medical Isotopes, Inc.
  • 2-3-4-Tri-O-benzoyl-α-L-fucopyranosyltrichloroacetimidate
  • 250 mg
  • $ 930.00
  • Biosynth Carbosynth
  • 2,3,4-Tri-O-benzoyl-a-L-fucopyranosyl trichloroacetimidate
  • 1 g
  • $ 1470.00
Total 2 raw suppliers
Chemical Property of 1,2,3-Tri-O-benzoyl-α-L-fucopyranose, Trichloroacetimidate
Chemical Property:
  • PSA:121.21000 
  • LogP:5.87180 
  • Solubility.:Chloroform, Dichloromethane, Ethyl Acetate 
Purity/Quality:

97% *data from raw suppliers

1,2,3-Tri-O-benzoyl-α-L-fucopyranose,Trichloroacetimidate *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Uses 1,2,3-Tri-O-benzoyl-α-L-fucopyranose, Trichloroacetimidate (cas# 180476-30-6) is a compound useful in organic synthesis.
Technology Process of 1,2,3-Tri-O-benzoyl-α-L-fucopyranose, Trichloroacetimidate

There total 5 articles about 1,2,3-Tri-O-benzoyl-α-L-fucopyranose, Trichloroacetimidate 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 1,8-diazabicyclo[5.4.0]undec-7-ene; lithium chloride; In acetonitrile; for 16h;
DOI:10.1080/07328309608005678
Guidance literature:
With 1,8-diazabicyclo[5.4.0]undec-7-ene; In dichloromethane; at 0 - 20 ℃;
DOI:10.1002/chem.201802577
Guidance literature:
Multi-step reaction with 2 steps
1: pyridine / 1 h / Ambient temperature
2: 95 percent / LiCl, DBU / acetonitrile / 16 h
With pyridine; 1,8-diazabicyclo[5.4.0]undec-7-ene; lithium chloride; In acetonitrile;
DOI:10.1080/07328309608005678
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