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2-Benzyloxy-3-Methoxy-6-nitrobenzaldehyde

Base Information
  • Chemical Name:2-Benzyloxy-3-Methoxy-6-nitrobenzaldehyde
  • CAS No.:2426-61-1
  • Molecular Formula:C15H13NO5
  • Molecular Weight:287.272
  • Hs Code.:
  • Mol file:2426-61-1.mol
2-Benzyloxy-3-Methoxy-6-nitrobenzaldehyde

Synonyms:2-(benzyloxy)-3-methoxy-6-nitrobenzaldehyde

Suppliers and Price of 2-Benzyloxy-3-Methoxy-6-nitrobenzaldehyde
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
  • 2-Benzyloxy-3-methoxy-6-nitrobenzaldehyde
  • 25mg
  • $ 165.00
  • Medical Isotopes, Inc.
  • 2-Benzyloxy-3-methoxy-6-nitrobenzaldehyde
  • 250 mg
  • $ 2200.00
Total 5 raw suppliers
Chemical Property of 2-Benzyloxy-3-Methoxy-6-nitrobenzaldehyde
Chemical Property:
  • Solubility.:DCM, Ethyl Acetate, Methanol 
Purity/Quality:

99% *data from raw suppliers

2-Benzyloxy-3-methoxy-6-nitrobenzaldehyde *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Uses 2-Benzyloxy-3-methoxy-6-nitrobenzaldehyde is an intermediate in the synthesis of 4-Hydroxymelatonin (H944635), a metabolite of Melatonin (M215000), a hormone found in animals that regulates sleep cycle.
Technology Process of 2-Benzyloxy-3-Methoxy-6-nitrobenzaldehyde

There total 4 articles about 2-Benzyloxy-3-Methoxy-6-nitrobenzaldehyde 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 potassium carbonate; In N,N-dimethyl-formamide; acetonitrile; at 100 ℃; for 4h;
DOI:10.1021/ol051286l DOI:10.1021/jo701987r
Guidance literature:
2-hydroxy-3-methoxy-6-nitrobenzaldehyde; With potassium carbonate; In acetonitrile; at 20 ℃; for 0.166667h;
benzyl chloride; With potassium iodide; In acetonitrile; for 2.5h; Reflux;
DOI:10.1016/j.ejmech.2009.07.012
Guidance literature:
Multi-step reaction with 2 steps
1: (i) NO2/HNO3, (ii) aq. KOH, MeOH
2: K2CO3 / dimethylformamide; dimethylsulfoxide
With potassium carbonate; In dimethyl sulfoxide; N,N-dimethyl-formamide;
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