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methyl 3-(acetylamino)-4-O-benzoyl-6-bromo-2,3,6-trideoxyhexopyranoside

Base Information
  • Chemical Name:methyl 3-(acetylamino)-4-O-benzoyl-6-bromo-2,3,6-trideoxyhexopyranoside
  • CAS No.:63554-16-5
  • Molecular Formula:C16H20 Br N O5
  • Molecular Weight:386.2377
  • Hs Code.:
methyl 3-(acetylamino)-4-O-benzoyl-6-bromo-2,3,6-trideoxyhexopyranoside

Synonyms:NSC276416

Suppliers and Price of methyl 3-(acetylamino)-4-O-benzoyl-6-bromo-2,3,6-trideoxyhexopyranoside
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
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Total 6 raw suppliers
Chemical Property of methyl 3-(acetylamino)-4-O-benzoyl-6-bromo-2,3,6-trideoxyhexopyranoside
Chemical Property:
  • Boiling Point:540.4°Cat760mmHg 
  • Flash Point:280.6°C 
  • Density:1.42g/cm3 
Purity/Quality:

85.0-99.8% *data from raw suppliers

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

SDS file from LookChem

Useful:
Technology Process of methyl 3-(acetylamino)-4-O-benzoyl-6-bromo-2,3,6-trideoxyhexopyranoside

There total 6 articles about methyl 3-(acetylamino)-4-O-benzoyl-6-bromo-2,3,6-trideoxyhexopyranoside 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 N-Bromosuccinimide; barium carbonate; In tetrachloromethane; for 6h; Heating;
DOI:10.1055/s-2000-6328
Guidance literature:
Multi-step reaction with 6 steps
1: NaBH4 / methanol / 2 h / 0 - 20 °C
2: pyridine / CH2Cl2 / 0.75 h / 20 °C
3: NaN3 / dimethylformamide / 1.5 h / 20 °C
4: LiAlH4 / tetrahydrofuran / 1 h / 0 °C
5: pyridine / 2 h / 20 °C
6: 75.9 percent / NBS; BaCO3 / CCl4 / 6 h / Heating
With pyridine; sodium tetrahydroborate; N-Bromosuccinimide; lithium aluminium tetrahydride; sodium azide; barium carbonate; In tetrahydrofuran; methanol; tetrachloromethane; dichloromethane; N,N-dimethyl-formamide; 1: Reduction / 2: Esterification / 3: Substitution / 4: Reduction / 5: Acetylation / 6: Substitution;
DOI:10.1055/s-2000-6328
Guidance literature:
Multi-step reaction with 3 steps
1: LiAlH4 / tetrahydrofuran / 1 h / 0 °C
2: pyridine / 2 h / 20 °C
3: 75.9 percent / NBS; BaCO3 / CCl4 / 6 h / Heating
With pyridine; N-Bromosuccinimide; lithium aluminium tetrahydride; barium carbonate; In tetrahydrofuran; tetrachloromethane; 1: Reduction / 2: Acetylation / 3: Substitution;
DOI:10.1055/s-2000-6328
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