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N-Hydroxy-5-((4-nitrophenyl)sulfonyl)-2-furancarboximidamide

Base Information
  • Chemical Name:N-Hydroxy-5-((4-nitrophenyl)sulfonyl)-2-furancarboximidamide
  • CAS No.:75745-74-3
  • Molecular Formula:C11H9N3O6S
  • Molecular Weight:311.275
  • Hs Code.:
  • Mol file:75745-74-3.mol
N-Hydroxy-5-((4-nitrophenyl)sulfonyl)-2-furancarboximidamide

Synonyms:BRN 4546911;N-Hydroxy-5-((4-nitrophenyl)sulfonyl)-2-furancarboximidamide;2-Furancarboximidamide, N-hydroxy-5-((4-nitrophenyl)sulfonyl)-;LS-70150

Suppliers and Price of N-Hydroxy-5-((4-nitrophenyl)sulfonyl)-2-furancarboximidamide
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
  • American Custom Chemicals Corporation
  • N-HYDROXY-5-((4-NITROPHENYL)SULFONYL)-2-FURAN CARBOXIMIDAMIDE 95.00%
  • 5MG
  • $ 502.59
Total 3 raw suppliers
Chemical Property of N-Hydroxy-5-((4-nitrophenyl)sulfonyl)-2-furancarboximidamide
Chemical Property:
  • PSA:160.09000 
  • LogP:3.41940 
  • XLogP3:1.4
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:7
  • Rotatable Bond Count:3
  • Exact Mass:311.02120619
  • Heavy Atom Count:21
  • Complexity:515
Purity/Quality:

99% *data from raw suppliers

N-HYDROXY-5-((4-NITROPHENYL)SULFONYL)-2-FURAN CARBOXIMIDAMIDE 95.00% *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:C1=CC(=CC=C1[N+](=O)[O-])S(=O)(=O)C2=CC=C(O2)C(=NO)N
  • Isomeric SMILES:C1=CC(=CC=C1[N+](=O)[O-])S(=O)(=O)C2=CC=C(O2)/C(=N\O)/N
Technology Process of N-Hydroxy-5-((4-nitrophenyl)sulfonyl)-2-furancarboximidamide

There total 2 articles about N-Hydroxy-5-((4-nitrophenyl)sulfonyl)-2-furancarboximidamide 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 hydroxide; hydroxylamine hydrochloride; In ethanol; for 3h; Heating;
Guidance literature:
Multi-step reaction with 2 steps
1: 54 percent / 46percent H2O2 / acetic acid / 75 h / Ambient temperature
2: 61 percent / NH2OH*HCl, KOH / ethanol / 3 h / Heating
With potassium hydroxide; hydroxylamine hydrochloride; dihydrogen peroxide; In ethanol; acetic acid;
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