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2-Methoxy-6-(methylsulfonyl)aniline

Base Information Edit
  • Chemical Name:2-Methoxy-6-(methylsulfonyl)aniline
  • CAS No.:148726-71-0
  • Molecular Formula:C8H11NO3S
  • Molecular Weight:201.246
  • Hs Code.:
  • European Community (EC) Number:845-791-0
  • DSSTox Substance ID:DTXSID50434497
  • Wikidata:Q82248933
  • Mol file:148726-71-0.mol
2-Methoxy-6-(methylsulfonyl)aniline

Synonyms:2-Methoxy-6-(methylsulfonyl)aniline;148726-71-0;2-methanesulfonyl-6-methoxyaniline;2-methoxy-6-methylsulfonylaniline;DTXSID50434497;AKOS016011043;EN300-130183;Z1509442799

Suppliers and Price of 2-Methoxy-6-(methylsulfonyl)aniline
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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  • price
Total 1 raw suppliers
Chemical Property of 2-Methoxy-6-(methylsulfonyl)aniline Edit
Chemical Property:
  • XLogP3:1
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:4
  • Rotatable Bond Count:2
  • Exact Mass:201.04596439
  • Heavy Atom Count:13
  • Complexity:257
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:COC1=C(C(=CC=C1)S(=O)(=O)C)N
Technology Process of 2-Methoxy-6-(methylsulfonyl)aniline

There total 6 articles about 2-Methoxy-6-(methylsulfonyl)aniline 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 hydrogen; palladium on activated charcoal; In ethyl acetate; for 1h; under 760 Torr;
DOI:10.1021/jm00063a014
Guidance literature:
Multi-step reaction with 6 steps
1: SOCl2
2: 1.) NaN3, 2.) H2O, 4.) NaOH, 5.) HCl
3: 1.) 98percent sulfuric acid, NaNO2, 2.) CuCl2, 36percent aq. HCl / 1.) acetic acid, 10 deg C, 1 h, 2.) acetic acid, RT, 1 h
4: 35 percent / dimethylformamide; H2O / 2 h / 100 °C
5: 61 percent / mcpba / CH2Cl2 / Ambient temperature
6: 99 percent / H2 / 10percent Pd/C / ethyl acetate / 1 h / 760 Torr
With hydrogenchloride; sodium hydroxide; thionyl chloride; sodium azide; sulfuric acid; water; hydrogen; 3-chloro-benzenecarboperoxoic acid; copper dichloride; sodium nitrite; palladium on activated charcoal; In dichloromethane; water; ethyl acetate; N,N-dimethyl-formamide;
DOI:10.1021/jm00063a014
Guidance literature:
Multi-step reaction with 3 steps
1: 35 percent / dimethylformamide; H2O / 2 h / 100 °C
2: 61 percent / mcpba / CH2Cl2 / Ambient temperature
3: 99 percent / H2 / 10percent Pd/C / ethyl acetate / 1 h / 760 Torr
With hydrogen; 3-chloro-benzenecarboperoxoic acid; palladium on activated charcoal; In dichloromethane; water; ethyl acetate; N,N-dimethyl-formamide;
DOI:10.1021/jm00063a014
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