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Trimethylammonium p-toluenesulfonate, also known as trimethylammonium tosylate or Me3NHOTs, is a quaternary ammonium salt derived from the reaction of trimethylamine and p-toluenesulfonic acid. It is a white crystalline solid that is soluble in water and organic solvents. trimethylammonium p-toluenesulfonate is widely used as a phase-transfer catalyst in organic synthesis, facilitating the transfer of reactants between aqueous and organic phases. It is also employed as a reagent in the preparation of various organic compounds, such as alkylation reactions, and as a mild acid catalyst in the synthesis of pharmaceuticals and other specialty chemicals. Trimethylammonium p-toluenesulfonate is known for its stability and ease of handling, making it a popular choice in the laboratory and industrial settings.

2840-23-5

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2840-23-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2840-23-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,8,4 and 0 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 2840-23:
(6*2)+(5*8)+(4*4)+(3*0)+(2*2)+(1*3)=75
75 % 10 = 5
So 2840-23-5 is a valid CAS Registry Number.

2840-23-5Downstream Products

2840-23-5Relevant academic research and scientific papers

SUBSTITUTION OF THE ANION IN AMMONIUM AND PHOSPHONIUM CHLORIDES BY THE ACTION OF ELECTROPHILIC AGENTS

Kukhar', V. P.,Pasternak, V. I.,Shevchenko, I. V.,Shevchenko, M. V.,Marchenko, A. P.,Makovetskii, Yu. P.

, p. 161 - 166 (2007/10/02)

N,N-Dialkylmethaniminium iodides were obtained by the reactions of N,N-dialkylmethaniminium chlorides with methyl iodide.The reactions of ammonium and phosphonium chlorides with triethyloxonium tetrafluoroborate, dimethyl sulfate, methyl tosylate, and methyl iodide take place with substitution of the chloride ion by the BF4-, CH3SO3O-, p-CH3C6H4SO3- or I- ions.Substitution of the chloride ion of phosphonium salts by the iodide ion can be realized by the action of trimethyliodosilane.

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