54664-52-7

Usage

Explanation

The compound's full name, which describes its structure and components.

Explanation

A shorter, more common name used to refer to the compound.

Explanation

It is a carbon-containing compound, which classifies it as an organic compound.

Explanation

The core structure of the compound, which consists of a triaza (three nitrogen atoms) and a diene (two double bonds) system.

Explanation

These groups are attached to the core structure, contributing to the compound's properties and reactivity.

Explanation

The presence of the 4-chlorophenyl group gives the compound aromatic characteristics, which can influence its chemical behavior.

Explanation

The sulfonyl group increases the compound's reactivity and provides additional functional groups for further chemical reactions.

Explanation

This structure imparts specific properties to the compound, making it suitable for various chemical reactions and transformations.

Explanation

CET has potential applications in these industries due to its unique properties and reactivity.

Explanation

The exact applications and properties of CET depend on the specific context and conditions in which it is used, such as the presence of other reactants or the reaction environment.

Type of Compound

Organic compound

Structure

Triaza-diene-2-ium

Substituents

Sulfonyl and 4-chlorophenyl

Aromatic Properties

4-chlorophenyl group

Reactivity and Functionality

Sulfonyl group

Unique Properties

Triaza-diene-2-ium structure

Applications

Pharmaceutical and chemical industries

Context-Dependent Properties

Specific applications and properties

Upstream product

• 76653-12-8 sodium 4-chloro-β-phenethylsulfonate 
• 6529-53-9 1-(2-bromoethyl)-4-chlorobenzene 
• 76653-13-9 4-chloro-β-phenethylsulfonyl chloride 

Downstream Products

• 76653-03-7 7-chloro-2,4-dihydro-2,1-benzothiazine 2,2-oxide 
• 1073-67-2 4-vinylbenzyl chloride 
• 17422-33-2 6-chloroindole 
• 52537-00-5 6-chloroindoline 
• 54664-55-0 4-chloro-6,7-dihydro-5H-cyclopenta[b]pyridine 

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.