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5-(3,4-Dimethoxyphenyl)tetrazole-2-acetic acid (3-chlorobenzylidene)hydrazide

Base Information
  • Chemical Name:5-(3,4-Dimethoxyphenyl)tetrazole-2-acetic acid (3-chlorobenzylidene)hydrazide
  • CAS No.:94772-03-9
  • Molecular Formula:C18H17ClN6O3
  • Molecular Weight:400.824
  • Hs Code.:
5-(3,4-Dimethoxyphenyl)tetrazole-2-acetic acid (3-chlorobenzylidene)hydrazide

Synonyms:BRN 4584579;5-(3,4-Dimethoxyphenyl)tetrazole-2-acetic acid (3-chlorobenzylidene)hydrazide;94772-03-9;2H-Tetrazole-2-acetic acid, 5-(3,4-dimethoxyphenyl)-, ((3-chlorophenyl)methylene)hydrazide;5-(3,4-Dimethoxyphenyl)-2H-tetrazole-2-acetic acid ((3-chlorophenyl)methylene)hydrazide

Suppliers and Price of 5-(3,4-Dimethoxyphenyl)tetrazole-2-acetic acid (3-chlorobenzylidene)hydrazide
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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Chemical Property of 5-(3,4-Dimethoxyphenyl)tetrazole-2-acetic acid (3-chlorobenzylidene)hydrazide
Chemical Property:
  • XLogP3:3.4
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:7
  • Rotatable Bond Count:7
  • Exact Mass:400.1050661
  • Heavy Atom Count:28
  • Complexity:540
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:COC1=C(C=C(C=C1)C2=NN(N=N2)CC(=O)NN=CC3=CC(=CC=C3)Cl)OC
  • Isomeric SMILES:COC1=C(C=C(C=C1)C2=NN(N=N2)CC(=O)N/N=C/C3=CC(=CC=C3)Cl)OC
Technology Process of 5-(3,4-Dimethoxyphenyl)tetrazole-2-acetic acid (3-chlorobenzylidene)hydrazide

There total 4 articles about 5-(3,4-Dimethoxyphenyl)tetrazole-2-acetic acid (3-chlorobenzylidene)hydrazide 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 4 steps
1: 70 percent / NaN3, NH4Cl / dimethylformamide / 127 °C
2: 70 percent / NaOEt / ethanol / 16 h / Heating
3: 65 percent / 99percent H2H4*H2O / ethanol / 8 h / Heating
4: 45 percent / AcOH / ethanol / Heating
With sodium azide; sodium ethanolate; ammonium chloride; hydrazine hydrate; acetic acid; In ethanol; N,N-dimethyl-formamide;
Guidance literature:
Multi-step reaction with 3 steps
1: 70 percent / NaOEt / ethanol / 16 h / Heating
2: 65 percent / 99percent H2H4*H2O / ethanol / 8 h / Heating
3: 45 percent / AcOH / ethanol / Heating
With sodium ethanolate; hydrazine hydrate; acetic acid; In ethanol;
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