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5-O-Desosaminylerythronolide A oxime

Base Information Edit
  • Chemical Name:5-O-Desosaminylerythronolide A oxime
  • CAS No.:53066-45-8
  • Molecular Formula:C31H56N2O11
  • Molecular Weight:632.792
  • Hs Code.:
  • Mol file:53066-45-8.mol
5-O-Desosaminylerythronolide A oxime

Synonyms:Oxacyclotetradecane,erythromycin deriv.; 3-Acetyl-5-O-desosaminylerythronolide A oxime

Suppliers and Price of 5-O-Desosaminylerythronolide A oxime
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 3 raw suppliers
Chemical Property of 5-O-Desosaminylerythronolide A oxime Edit
Chemical Property:
  • Vapor Pressure:3.85E-26mmHg at 25°C 
  • Boiling Point:752.6°C at 760 mmHg 
  • PKA:11.95±0.70(Predicted) 
  • Flash Point:408.9°C 
  • PSA:187.81000 
  • Density:1.27g/cm3 
  • LogP:1.69230 
  • Solubility.:Dichloromethane, Chloroform, Methanol 
Purity/Quality:

99% *data from raw suppliers

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

SDS file from LookChem

Useful:
  • Uses 5-O-Desosaminylerythronolide A Oxime is an intermediate in synthesizing Erythrolosamine (E649910), a derivative of Erythromycin A Oxime (E650010), which displays no antibacterial activity. It is a potent precursor of ketolide antibiotics.
Technology Process of 5-O-Desosaminylerythronolide A oxime

There total 1 articles about 5-O-Desosaminylerythronolide A oxime 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:
Acetoxim 4, Acetanhydrid;
DOI:10.1021/jm00255a009
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