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Methylpyridinium tosylate

Base Information
  • Chemical Name:Methylpyridinium tosylate
  • CAS No.:38542-71-1
  • Molecular Formula:C13H16NO3S+
  • Molecular Weight:265.333
  • Hs Code.:
  • DSSTox Substance ID:DTXSID10959414
  • NSC Number:249267
Methylpyridinium tosylate

Synonyms:38542-71-1;methylpyridinium tosylate;n-methylpyridinium tosylate;SCHEMBL1982598;DTXSID10959414;OVFJVGPVSMMTSA-UHFFFAOYSA-M;NSC249267;NSC-249267;1-Methylpyridin-1-ium 4-methylbenzene-1-sulfonate

Suppliers and Price of Methylpyridinium tosylate
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
Total 5 raw suppliers
Chemical Property of Methylpyridinium tosylate
Chemical Property:
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:0
  • Exact Mass:265.07726451
  • Heavy Atom Count:18
  • Complexity:239
Purity/Quality:

99% *data from raw suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:CC1=CC=C(C=C1)S(=O)(=O)[O-].C[N+]1=CC=CC=C1
Technology Process of Methylpyridinium tosylate

There total 1 articles about Methylpyridinium tosylate 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:
In acetonitrile; for 24h; Inert atmosphere; Reflux;
DOI:10.1039/b906409e
Guidance literature:
With Dowex 1-X8 (Cl) 100-200 mesh standard grade resin; In water; Inert atmosphere;
DOI:10.1039/b906409e
Guidance literature:
N-methylpyridinium p-toluenesulfonate; With triphenylphosphine ditriflate; In dichloromethane; for 0.5h;
1,3,5-trimethyl-benzene; In dichloromethane; at 0 - 20 ℃; for 0.5h; chemoselective reaction;
DOI:10.1007/s13738-011-0062-3
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