54664-50-5

Usage

Chemical structure

A complex chemical compound with a triaza-1,2-dien-2-ium core and a sulfonyl group attached to a 2-phenylethyl group.

Charge

Likely has a positive charge due to the presence of the triaza-1,2-dien-2-ium moiety.

Potential applications

May have potential applications in pharmaceuticals or organic synthesis due to its unique structure and potential reactivity.

Further research

Additional research and analysis would be necessary to fully understand the properties and potential uses of 1-[(2-phenylethyl)sulfonyl]triaza-1,2-dien-2-ium.

Core component

Contains a triaza-1,2-dien-2-ium core, which is a heterocyclic compound with three nitrogen atoms.

Sulfonyl group

The sulfonyl group is attached to a 2-phenylethyl group, which is a phenyl group connected to an ethyl group.

Phenyl group

The phenyl group is a six-membered aromatic ring with alternating single and double carbon-carbon bonds.

Ethyl group

The ethyl group is a two-carbon chain with a methyl group (CH3) and a methylene group (CH2) connected to the phenyl group.

Reactivity

The compound's reactivity is not fully known, but its unique structure suggests it may have potential for use in chemical reactions.

Analysis

Further analysis would be needed to determine the compound's stability, solubility, and other physical and chemical properties.

Upstream product

• 4025-71-2 2-phenylethylsulfonyl chloride 

Downstream Products

• 3192-06-1 3,4-dihydro-1H-benzo[c][1,2]thiazine 2,2-dioxide 
• 16993-47-8 2-(phenyl)ethanesulfonamide 
• 76653-09-3 N-cyclohexyl-β-phenethylsulfonamide 
• 100-42-5 styrene 
• 120-72-9 indole 
• 496-15-1 1-indoline 
• 533-37-9 2,3-cyclopentenopyridine 
• 76653-10-6 N-phenyl-β-phenethylsulfonamide 
• 76653-08-2 N-(β-phenethylsulfonyl)azepine 

Relevant academic research and scientific papers

Thermolysis of Sulfonyl Azides Bearing Nucleophilic Neighboring Groups. A Search for Anchimeric Assistance

In a search for anchimeric assistance by n- or ?-donor neighboring groups in sulfonyl azide decompositions, 25 sulfonyl azides have been prepared and thermolyzed in 1-chloronaphthalene.First-order rate constants at 135 and 165 deg C were determined by mea

The Decomposition of β-Phenethylsulfonyl Azides. Solution Chemistry and Flash Vacuum Pyrolysis

The intramolecular cyclization of the parent title compound and a number of para-substituted derivatives (1) in solution was found to take place in low yield and to be accompanied by products of intermolecular reactions, namely, C-H insertion (4) and hydrogen abstraction (3).The use of an excess of a relatively inert solvent Freon 113 led to a better yield of the desired 3,4-dihydro-2,1-benzothiazine 2,2-dioxides (2).Flash vacuum pyrolysis (FVP) of 1 at 250-300 deg C also gave some 2, but the use of higher temperatures led to the formation of styrenes (8), indolines (9), indoles (10), sulfur dioxide, and the remarkable transformation products, the 4-substituted 6,7-dihydro-5H-1-pyrindines (7), in good yield.The styrenes result from the elimination of HN3 and SO2 from the azides, and indolines are formed in good yield by FVP of 2 at 650 deg C.The dihydropyrindines are not obtained from 2, and β-phenethynitrene is not a source of any of the above observed products.A mechanism is proposed for the formation of 7 from β-arylethylsulfonylnitrenes.Consistent with the mechanism is the observation that both 1- and 2-phenylpropanesulfonyl azide give a mixture of 6- and 7-methyl-6,7-dihydro-5H-1-pyrindines in the same ratio on FVP at 650 deg C.Thermolysis of 1a in benzene at 100 deg C gives an N-sulfonylazepine derivative.The FVP of 1 and 2 at 650 deg C are preparative routes to 7 and 9, respectively.