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4-(4-Hydroxyphenyl)sulfonylfuran-2-sulfonamide

Base Information Edit
  • Chemical Name:4-(4-Hydroxyphenyl)sulfonylfuran-2-sulfonamide
  • CAS No.:128348-44-7
  • Molecular Formula:C10H9NO6S2
  • Molecular Weight:303.317
  • Hs Code.:
  • ChEMBL ID:CHEMBL333747
  • DSSTox Substance ID:DTXSID30872217
  • Nikkaji Number:J513.635K
  • Mol file:128348-44-7.mol
4-(4-Hydroxyphenyl)sulfonylfuran-2-sulfonamide

Synonyms:128348-44-7;CHEMBL333747;DTXSID30872217;4-(4-Hydroxybenzene-1-sulfonyl)furan-2-sulfonamide

Suppliers and Price of 4-(4-Hydroxyphenyl)sulfonylfuran-2-sulfonamide
Supply Marketing:Edit
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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Total 0 raw suppliers
Chemical Property of 4-(4-Hydroxyphenyl)sulfonylfuran-2-sulfonamide Edit
Chemical Property:
  • XLogP3:-0.1
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:7
  • Rotatable Bond Count:3
  • Exact Mass:302.98712935
  • Heavy Atom Count:19
  • Complexity:509
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:C1=CC(=CC=C1O)S(=O)(=O)C2=COC(=C2)S(=O)(=O)N
Technology Process of 4-(4-Hydroxyphenyl)sulfonylfuran-2-sulfonamide

There total 5 articles about 4-(4-Hydroxyphenyl)sulfonylfuran-2-sulfonamide 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 boron tribromide; In dichloromethane; 1,2-dichloro-ethane; for 16h; Heating;
DOI:10.1002/jhet.5570270202
Guidance literature:
Multi-step reaction with 5 steps
1: 1.) n-butyllithium / 1.) ether, hexane, -78 deg C, 45 min, 2.) ether, hexane, from -78 deg C to RT, overnight
2: m-chloroperbenzoic acid (MCPBA) / CHCl3 / 1.5 h / 0 - 10 °C
3: chlorosulfonic acid, PCl5 / 0.42 h / 55 °C
4: NH3 (gas) / CHCl3 / 16 h / Ambient temperature
5: boron tribromide / 1,2-dichloro-ethane; CH2Cl2 / 16 h / Heating
With chlorosulfonic acid; n-butyllithium; phosphorus pentachloride; ammonia; boron tribromide; 3-chloro-benzenecarboperoxoic acid; In dichloromethane; chloroform; 1,2-dichloro-ethane;
DOI:10.1021/jm00099a010
Guidance literature:
Multi-step reaction with 4 steps
1: m-chloroperbenzoic acid (MCPBA) / CHCl3 / 1.5 h / 0 - 10 °C
2: chlorosulfonic acid, PCl5 / 0.42 h / 55 °C
3: NH3 (gas) / CHCl3 / 16 h / Ambient temperature
4: boron tribromide / 1,2-dichloro-ethane; CH2Cl2 / 16 h / Heating
With chlorosulfonic acid; phosphorus pentachloride; ammonia; boron tribromide; 3-chloro-benzenecarboperoxoic acid; In dichloromethane; chloroform; 1,2-dichloro-ethane;
DOI:10.1021/jm00099a010
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