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4-(4-Methoxybenzoyl)-2-furansulfonamide

Base Information
  • Chemical Name:4-(4-Methoxybenzoyl)-2-furansulfonamide
  • CAS No.:118993-61-6
  • Molecular Formula:C12H11NO5S
  • Molecular Weight:281.28400
  • Hs Code.:
  • ChEMBL ID:CHEMBL340519
  • DSSTox Substance ID:DTXSID00872204
  • Nikkaji Number:J277.482H
  • Wikidata:Q70000064
  • Mol file:118993-61-6.mol
4-(4-Methoxybenzoyl)-2-furansulfonamide

Synonyms:118993-61-6;4-(4-Methoxybenzoyl)-2-furansulfonamide;4-(4-methoxybenzoyl)furan-2-sulfonamide;CHEMBL340519;SCHEMBL10369217;DTXSID00872204

Suppliers and Price of 4-(4-Methoxybenzoyl)-2-furansulfonamide
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
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Total 1 raw suppliers
Chemical Property of 4-(4-Methoxybenzoyl)-2-furansulfonamide
Chemical Property:
  • PSA:107.98000 
  • LogP:2.94770 
  • XLogP3:1.5
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:6
  • Rotatable Bond Count:4
  • Exact Mass:281.03579362
  • Heavy Atom Count:19
  • Complexity:422
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:COC1=CC=C(C=C1)C(=O)C2=COC(=C2)S(=O)(=O)N
Technology Process of 4-(4-Methoxybenzoyl)-2-furansulfonamide

There total 5 articles about 4-(4-Methoxybenzoyl)-2-furansulfonamide 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 ammonia; In chloroform; for 16h; Ambient temperature;
DOI:10.1002/jhet.5570260648
Guidance literature:
With NH3 (gas); In tetrahydrofuran; N-methyl-acetamide; chloroform;
Guidance literature:
Multi-step reaction with 4 steps
1: 1.) n-BuLi, 3.) aq. HCl
2: H2SO4, acetic anhydride / CH2Cl2 / 72 h / Ambient temperature
3: oxalyl chloride, N,N-dimethylformamide / ethyl acetate / 16 h / Ambient temperature
4: NH3 (gas) / CHCl3 / 2 h / Ambient temperature
With hydrogenchloride; n-butyllithium; oxalyl dichloride; sulfuric acid; ammonia; acetic anhydride; N,N-dimethyl-formamide; In dichloromethane; chloroform; ethyl acetate;
DOI:10.1021/jm00099a010
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