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Methyl 3-azido-4,6-O-benzylidene-2,3-dideoxyhexopyranoside

Base Information
  • Chemical Name:Methyl 3-azido-4,6-O-benzylidene-2,3-dideoxyhexopyranoside
  • CAS No.:6386-19-2
  • Molecular Formula:C14H17 N3 O4
  • Molecular Weight:292.3099
  • Hs Code.:
  • DSSTox Substance ID:DTXSID20411199,DTXSID80978435
  • NSC Number:287056,287048
Methyl 3-azido-4,6-O-benzylidene-2,3-dideoxyhexopyranoside

Synonyms:62774-39-4;6386-19-2;AC1NQJIO;DTXSID20411199;DTXSID80978435;Methyl 3-azido-4,6-O-benzylidene-2,3-dideoxyhexopyranoside;NSC287048;NSC287056;NSC-287048;NSC-287056

Suppliers and Price of Methyl 3-azido-4,6-O-benzylidene-2,3-dideoxyhexopyranoside
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 2 raw suppliers
Chemical Property of Methyl 3-azido-4,6-O-benzylidene-2,3-dideoxyhexopyranoside
Chemical Property:
  • Boiling Point:°Cat760mmHg 
  • Flash Point:°C 
  • PSA:86.67000 
  • Density:g/cm3 
  • LogP:1.99366 
  • XLogP3:2.4
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:6
  • Rotatable Bond Count:3
  • Exact Mass:291.12190603
  • Heavy Atom Count:21
  • Complexity:396
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:COC1CC(C2C(O1)COC(O2)C3=CC=CC=C3)N=[N+]=[N-]
Technology Process of Methyl 3-azido-4,6-O-benzylidene-2,3-dideoxyhexopyranoside

There total 1 articles about Methyl 3-azido-4,6-O-benzylidene-2,3-dideoxyhexopyranoside 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:
Multi-step reaction with 2 steps
1: 76 percent / N-bromosuccinimide, barium carbonate / CCl4
2: 1.) H2, triethylamine / 1.) Raney nickel / 1.) methanol, 2.) methanol, 3.) methanol
With N-Bromosuccinimide; hydrogen; triethylamine; barium carbonate; nickel; In tetrachloromethane;
DOI:10.1248/cpb.30.1929
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