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N-amino-1-methyl-1,2,4-triazolium tosylate is a complex organic compound with the chemical formula C5H9N4O2S. It is a derivative of the 1,2,4-triazole ring system, which is a five-membered heterocyclic ring containing three nitrogen atoms and one carbon atom. The compound features a methyl group attached to the nitrogen atom at position 1, and an amino group at the same position, which is protonated, making it a cationic species. The tosylate group, which is a toluene sulfonate anion (C7H7SO3-), is attached to the cation, providing the overall charge neutrality to the molecule. N-amino-1-methyl-1,2,4-triazolium tosylate is of interest in organic chemistry and may have applications in the synthesis of various pharmaceuticals and chemical compounds due to its unique structure and reactivity.

6086-02-8

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6086-02-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6086-02-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,0,8 and 6 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 6086-02:
(6*6)+(5*0)+(4*8)+(3*6)+(2*0)+(1*2)=88
88 % 10 = 8
So 6086-02-8 is a valid CAS Registry Number.

6086-02-8Relevant academic research and scientific papers

Alkylaminonitrobenzenes by Vicarious Nucleophilic Amination with 4-(Alkylamino)-1,2,4-triazoles

Katritzky, Alan R.,Laurenzo, Kathleen S.

, p. 3978 - 3982 (2007/10/02)

A series of 4-(alkylamino)-1,2,4-triazoles transfer the alkylamino group to the 4-position of nitrobenzene and various 3-substituted nitrobenzenes, with no detectable ortho substitution.By contrast 2-nitrothiophene reacts in the 3-position and 2-nitronaphthalene in the 1-position; 1-nitronaphthalene gives a mixture of products derived from dominant 2- with some 4-substitution.The orientations are discussed and rationalized.

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