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3,4-Dimethoxythioanisole

Base Information
  • Chemical Name:3,4-Dimethoxythioanisole
  • CAS No.:2570-43-6
  • Molecular Formula:C9H12O2S
  • Molecular Weight:184.259
  • Hs Code.:
  • European Community (EC) Number:673-600-9
  • DSSTox Substance ID:DTXSID00948574
  • Nikkaji Number:J1.809.806G
  • Wikidata:Q82926400
  • Mol file:2570-43-6.mol
3,4-Dimethoxythioanisole

Synonyms:3,4-Dimethoxythioanisole;2570-43-6;1,2-dimethoxy-4-methylsulfanylbenzene;1,2-dimethoxy-4-(methylsulfanyl)benzene;(3,4-dimethoxyphenyl)(methyl)sulfane;3,4-Dimethoxythioanisol;SCHEMBL3511079;DTXSID00948574;1-(Methylthio)-3,4-dimethoxybenzene;AKOS006278641;E97742

Suppliers and Price of 3,4-Dimethoxythioanisole
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
  • 3,4-DIMETHOXYTHIOANISOLE 98.00%
  • 50G
  • $ 2933.70
  • AHH
  • 3,4-Dimethoxythioanisole 98%
  • 50g
  • $ 290.00
Total 10 raw suppliers
Chemical Property of 3,4-Dimethoxythioanisole
Chemical Property:
  • PSA:43.76000 
  • LogP:2.42570 
  • XLogP3:2.6
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:3
  • Exact Mass:184.05580079
  • Heavy Atom Count:12
  • Complexity:130
Purity/Quality:

98%min *data from raw suppliers

3,4-DIMETHOXYTHIOANISOLE 98.00% *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:COC1=C(C=C(C=C1)SC)OC
Technology Process of 3,4-Dimethoxythioanisole

There total 13 articles about 3,4-Dimethoxythioanisole 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; In ethanol; for 0.5h; Inert atmosphere; Reflux;
DOI:10.1021/jacs.0c11420
Guidance literature:
4-Bromoveratrole; With n-butyllithium; In tetrahydrofuran; hexane; at -78 ℃; for 1h; Inert atmosphere;
Dimethyldisulphide; In tetrahydrofuran; hexane; at -78 - 20 ℃; for 12h; Inert atmosphere;
DOI:10.1021/jacs.1c00529
Guidance literature:
carbon dioxide; 3,4-dimethoxythiophenol; With sodium tetrahydroborate; 18-crown-6 ether; at 80 ℃; for 0.5h; under 76.0051 Torr; Schlenk technique; Sealed tube;
With iodine; at 140 ℃; for 12h; Schlenk technique; Sealed tube;
DOI:10.1021/acs.joc.9b01180
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