2-Chloro-1-methylpyridinium trifluoromethanesulphonate

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2-Chloro-1-methylpyridinium trifluoromethanesulphonate

  • Name 2-Chloro-1-methylpyridinium trifluoromethanesulphonate
  • CAS 84030-18-2
  • Purity 99%
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Product Details

Reputable manufacturer supply 2-Chloro-1-methylpyridinium trifluoromethanesulphonate 84030-18-2 in stock with high standard

  • Molecular Formula: CF3O3S*C6H7ClN
  • Molecular Weight: 277.652
  • PSA: 69.46000 
  • LogP: 2.29670 

2-Chloro-1-methylpyridinium trifluoromethanesulphonate(Cas 84030-18-2) Usage

General Description

2-Chloro-1-methylpyridinium trifluoromethanesulphonate is a chemical compound that is used as a reagent in organic synthesis. It is an effective source of the 2-chloro-1-methylpyridinium cation, which can be utilized in a variety of reactions including the synthesis of pharmaceutical compounds and agrochemicals. The trifluoromethanesulphonate anion in the compound provides stability and solubility, making it a valuable tool in chemical research and development. Additionally, it is known for its mild and selective reactivity, making it a popular choice in the pharmaceutical industry for the synthesis of complex molecules. The compound is also known for its high purity, which makes it a reliable and efficient reagent for chemical reactions.

InChI:InChI=1/C6H7ClN.CHF3O3S/c1-8-5-3-2-4-6(8)7;2-1(3,4)8(5,6)7/h2-5H,1H3;(H,5,6,7)/q+1;/p-1

84030-18-2 Relevant articles

Synthesis of new Pro-PYE ligands as co-catalysts toward Pd-catalyzed Heck-Mizoroki cross coupling reactions

Munir, Naima,Masood, Sara,Liaqat, Faroha,Tahir, Muhammad Nawaz,Yousuf, Sammer,Kalsoom, Saima,Mughal, Ehsan Ullah,Sumrra, Sajjad Hussain,Maalik, Aneela,Zafar, Muhammad Naveed

, p. 37986 - 38000 (2019/12/03)

The present research work describes the ...

Organocatalytic enantioselective synthesis of bicyclic β-lactones from aldehyde acids via nucleophile-catalyzed aldollactonization (NCAL)

Nguyen, Henry,Oh, Seongho,Henry-Riyad, Huda,Sepulveda, Diana,Romo, Daniel

, p. 121 - 137 (2014/04/03)

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Pyridine-derived N-heterocyclic carbenes: An experimental and theoretical evaluation of the bonding in and reactivity of selected normal and abnormal complexes of nickel(II) and palladium(II)

Stander-Grobler, Elzet,Schuster, Oliver,Heydenrych, Greta,Cronje, Stephanie,Tosh, Evangeline,Albrecht, Martin,Frenking, Gernot,Raubenheimer, Helgard G.

experimental part, p. 5821 - 5833 (2011/02/22)

We report a thorough investigation of a ...

Preparation of Mono-/Difluorinated Hydrocarbon Compounds

-

Page/Page column 7, (2009/09/28)

Mono- or difluorinated hydrocarbon compo...

84030-18-2 Process route

2-chloropyridine
109-09-1

2-chloropyridine

methyl trifluoromethanesulfonate
333-27-7

methyl trifluoromethanesulfonate

N-methyl-2-chloropyridinium trifluoromethanesulfonate
84030-18-2

N-methyl-2-chloropyridinium trifluoromethanesulfonate

Conditions
Conditions Yield
In toluene; at 20 ℃; for 1h;
99%
In dichloromethane; Schlenk technique; Inert atmosphere;
95%
In dichloromethane; at -78 - 20 ℃; for 16h;
94%
In dichloromethane; at -78 - 23 ℃; for 12.1667h; Inert atmosphere;
93%
In dichloromethane; at 20 ℃; for 18h;
88%

84030-18-2 Upstream products

  • 109-09-1
    109-09-1

    2-chloropyridine

  • 333-27-7
    333-27-7

    methyl trifluoromethanesulfonate

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