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3-(BENZYLOXY)BENZALDEHYDE OXIME

Base Information
  • Chemical Name:3-(BENZYLOXY)BENZALDEHYDE OXIME
  • CAS No.:93033-58-0
  • Molecular Formula:C14H13NO2
  • Molecular Weight:227.263
  • Hs Code.:2928000090
  • Mol file:93033-58-0.mol
3-(BENZYLOXY)BENZALDEHYDE OXIME

Synonyms:m-benzyloxybenzaldehyde oxime;

Suppliers and Price of 3-(BENZYLOXY)BENZALDEHYDE OXIME
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
  • Crysdot
  • 3-(Benzyloxy)benzaldehydeoxime 97%
  • 5g
  • $ 904.00
  • Aronis compounds
  • 3-(benzyloxy)benzaldehydeoxime
  • 20mg
  • $ 30.00
  • American Custom Chemicals Corporation
  • 3-(BENZYLOXY)BENZALDEHYDE OXIME 95.00%
  • 5G
  • $ 1295.03
  • American Custom Chemicals Corporation
  • 3-(BENZYLOXY)BENZALDEHYDE OXIME 95.00%
  • 2.5G
  • $ 1065.66
  • American Custom Chemicals Corporation
  • 3-(BENZYLOXY)BENZALDEHYDE OXIME 95.00%
  • 1G
  • $ 765.23
Total 4 raw suppliers
Chemical Property of 3-(BENZYLOXY)BENZALDEHYDE OXIME
Chemical Property:
  • PSA:41.82000 
  • LogP:3.07370 
Purity/Quality:

99% *data from raw suppliers

3-(Benzyloxy)benzaldehydeoxime 97% *data from reagent suppliers

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

SDS file from LookChem

Useful:
Technology Process of 3-(BENZYLOXY)BENZALDEHYDE OXIME

There total 4 articles about 3-(BENZYLOXY)BENZALDEHYDE 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:
With sodium hydroxide; hydroxylamine hydrochloride; In ethanol; at 0 - 20 ℃;
DOI:10.1002/jccs.200400093
Guidance literature:
Multi-step reaction with 2 steps
1: 92 percent / K2CO3; KI / tetrahydrofuran / 6 h / Heating
2: 89 percent / hydroxylamine; acetic acid / ethanol / 3 h / Heating
With hydroxylamine; potassium carbonate; acetic acid; potassium iodide; In tetrahydrofuran; ethanol;
DOI:10.1016/j.bmc.2004.12.026
Guidance literature:
Multi-step reaction with 2 steps
1: 92 percent / K2CO3; KI / tetrahydrofuran / 6 h / Heating
2: 89 percent / hydroxylamine; acetic acid / ethanol / 3 h / Heating
With hydroxylamine; potassium carbonate; acetic acid; potassium iodide; In tetrahydrofuran; ethanol;
DOI:10.1016/j.bmc.2004.12.026
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