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2-Ethoxybenzenesulfonamide

Base Information Edit
  • Chemical Name:2-Ethoxybenzenesulfonamide
  • CAS No.:58734-61-5
  • Molecular Formula:C8H11NO3S
  • Molecular Weight:201.246
  • Hs Code.:
  • DSSTox Substance ID:DTXSID80599023
  • Wikidata:Q82494859
  • Mol file:58734-61-5.mol
2-Ethoxybenzenesulfonamide

Synonyms:2-Ethoxybenzenesulfonamide;58734-61-5;2-ethoxybenzene-1-sulfonamide;ethoxy-benzene sulfonamide;SCHEMBL5579618;DTXSID80599023;BENZENESULFONAMIDE, 2-ETHOXY-;AKOS013257957;SB78076;DB-285472;CS-0232020;EN300-126122;F53486;F2158-2256

Suppliers and Price of 2-Ethoxybenzenesulfonamide
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
  • Packaging
  • price
  • TRC
  • 2-ethoxybenzenesulfonamide
  • 50mg
  • $ 220.00
  • American Custom Chemicals Corporation
  • 2-ETHOXY-BENZENESULFONAMIDE 95.00%
  • 5MG
  • $ 502.28
  • AK Scientific
  • 2-Ethoxybenzenesulfonamide
  • 500mg
  • $ 700.00
Total 1 raw suppliers
Chemical Property of 2-Ethoxybenzenesulfonamide Edit
Chemical Property:
  • PSA:77.77000 
  • LogP:2.51380 
  • XLogP3:0.4
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:4
  • Rotatable Bond Count:3
  • Exact Mass:201.04596439
  • Heavy Atom Count:13
  • Complexity:245
Purity/Quality:

99% *data from raw suppliers

2-ethoxybenzenesulfonamide *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:CCOC1=CC=CC=C1S(=O)(=O)N
Technology Process of 2-Ethoxybenzenesulfonamide

There total 1 articles about 2-Ethoxybenzenesulfonamide 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:
2-hydroxybenzenesulfonamide; With potassium carbonate; In N,N-dimethyl-formamide; at 20 ℃; for 0.5h; Reflux;
ethyl iodide; In N,N-dimethyl-formamide; Reflux;
DOI:10.1021/acs.jafc.1c02081
Guidance literature:
With dmap; triethylamine; In dichloromethane; ethyl acetate; at 0 - 20 ℃; for 24h; Inert atmosphere; Schlenk technique;
DOI:10.1021/acs.orglett.6b01954
Guidance literature:
With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In dichloromethane; for 4h;
DOI:10.1021/acs.jmedchem.0c01116
upstream raw materials:

2-hydroxybenzenesulfonamide

ethyl iodide

Downstream raw materials:

2-ethoxybenzenethiol

Refernces Edit
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