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4,5-Dimethoxy-2-nitrobenzaldehyde oxime

Base Information
  • Chemical Name:4,5-Dimethoxy-2-nitrobenzaldehyde oxime
  • CAS No.:29577-51-3
  • Molecular Formula:C9H10N2O5
  • Molecular Weight:226.189
  • Hs Code.:
  • DSSTox Substance ID:DTXSID30430533
  • Mol file:29577-51-3.mol
4,5-Dimethoxy-2-nitrobenzaldehyde oxime

Synonyms:4,5-Dimethoxy-2-nitrobenzaldehyde oxime;ST019349;29577-51-3;DTXSID30430533;CRQFTYUZLLSSDF-BJMVGYQFSA-N;AKOS000485327;4,5-Dimethoxy-2-nitrobenzaldehyde oxime #;Benzaldehyde, 4,5-dimethoxy-2-nitro-, oxime

Suppliers and Price of 4,5-Dimethoxy-2-nitrobenzaldehyde 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
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  • 4,5-dimethoxy-2-nitrobenzaldehydeoxime
  • 5mg
  • $ 15.00
Total 0 raw suppliers
Chemical Property of 4,5-Dimethoxy-2-nitrobenzaldehyde oxime
Chemical Property:
  • PSA:96.87000 
  • LogP:1.94330 
  • XLogP3:1.4
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:6
  • Rotatable Bond Count:3
  • Exact Mass:226.05897142
  • Heavy Atom Count:16
  • Complexity:265
Purity/Quality:

4,5-dimethoxy-2-nitrobenzaldehydeoxime *data from reagent suppliers

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

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:
  • Canonical SMILES:COC1=C(C=C(C(=C1)C=NO)[N+](=O)[O-])OC
  • Isomeric SMILES:COC1=C(C=C(C(=C1)/C=N/O)[N+](=O)[O-])OC
Technology Process of 4,5-Dimethoxy-2-nitrobenzaldehyde oxime

There total 1 articles about 4,5-Dimethoxy-2-nitrobenzaldehyde 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 pyridine; hydroxylamine hydrochloride; In ethanol; for 8h; Reflux;
DOI:10.1039/c1pp05308f
Guidance literature:
With triethylamine; In dichloromethane; for 2h;
DOI:10.1021/jo9917846
Guidance literature:
2-nitro-4,5-dimethoxybenzaldehyde oxime; With N-chloro-succinimide; In N,N-dimethyl-formamide; for 3h;
propargyl alcohol; With copper(ll) sulfate pentahydrate; potassium carbonate; ascorbic acid; In N,N-dimethyl-formamide; for 1h;
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