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Benzoic acid, 4-ethoxy-, 2-(2H-1,4-benzoxazin-3-yl)hydrazide

Base Information
  • Chemical Name:Benzoic acid, 4-ethoxy-, 2-(2H-1,4-benzoxazin-3-yl)hydrazide
  • CAS No.:78959-34-9
  • Molecular Formula:C17H17N3O3
  • Molecular Weight:311.34
  • Hs Code.:
  • DSSTox Substance ID:DTXSID40229435
  • Wikidata:Q83109686
Benzoic acid, 4-ethoxy-, 2-(2H-1,4-benzoxazin-3-yl)hydrazide

Synonyms:BRN 4534066;Benzoic acid, 4-ethoxy-, 2-(2H-1,4-benzoxazin-3-yl)hydrazide;78959-34-9;4-Ethoxybenzoic acid 2-(2H-1,4-benzoxazin-3-yl)hydrazide;DTXSID40229435;LS-37351

Suppliers and Price of Benzoic acid, 4-ethoxy-, 2-(2H-1,4-benzoxazin-3-yl)hydrazide
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of Benzoic acid, 4-ethoxy-, 2-(2H-1,4-benzoxazin-3-yl)hydrazide
Chemical Property:
  • XLogP3:2.5
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:4
  • Rotatable Bond Count:5
  • Exact Mass:311.12699141
  • Heavy Atom Count:23
  • Complexity:433
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CCOC1=CC=C(C=C1)C(=O)NNC2=NC3=CC=CC=C3OC2
Technology Process of Benzoic acid, 4-ethoxy-, 2-(2H-1,4-benzoxazin-3-yl)hydrazide

There total 3 articles about Benzoic acid, 4-ethoxy-, 2-(2H-1,4-benzoxazin-3-yl)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 2 steps
1: K2CO3 / acetone / 8 h / Heating
2: 60 percent / ethanol / Ambient temperature
With potassium carbonate; In ethanol; acetone;
Guidance literature:
Multi-step reaction with 3 steps
1: 90 percent / P2S5/Et3N / acetonitrile
2: K2CO3 / acetone / 8 h / Heating
3: 60 percent / ethanol / Ambient temperature
With tetraphosphorus decasulfide; potassium carbonate; triethylamine; In ethanol; acetone; acetonitrile;
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