41335-62-0

Basic information

• Product Name: 2-[2-(4-chlorophenyl)-2-oxoethyl]-1,2-benzisothiazol-3(2H)-one 1,1-dioxide
• Synonyms: 2-[2-(4-chlorophenyl)-2-oxoethyl]-1,2-benzisothiazol-3(2H)-one 1,1-dioxide
• CAS NO: 41335-62-0
• Molecular Weight: 335.768
• Mol File: 41335-62-0.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: 2-[2-(4-chlorophenyl)-2-oxoethyl]-1,2-benzisothiazol-3(2H)-one 1,1-dioxide(CAS DataBase Reference)
• NIST Chemistry Reference: 2-[2-(4-chlorophenyl)-2-oxoethyl]-1,2-benzisothiazol-3(2H)-one 1,1-dioxide(41335-62-0)
• EPA Substance Registry System: 2-[2-(4-chlorophenyl)-2-oxoethyl]-1,2-benzisothiazol-3(2H)-one 1,1-dioxide(41335-62-0)

Safety Data

• Hazardous Substances Data: 41335-62-0(Hazardous Substances Data)

Usage

Molecular structure

2-[2-(4-chlorophenyl)-2-oxoethyl]-1,2-benzisothiazol-3(2H)-one 1,1-dioxide consists of a benzisothiazolone ring, a chlorophenyl group, a 2-oxoethyl group, and a 1,1-dioxide moiety.

Benzisothiazolone ring

A heterocyclic ring structure containing sulfur and nitrogen atoms, which contributes to the compound's chemical stability and potential applications.

Chlorophenyl group

A phenyl ring with a chlorine atom attached, which may influence the compound's reactivity, solubility, and biological activity.

2-Oxoethyl group

A two-carbon functional group with a ketone (C=O) moiety, which can participate in various chemical reactions and contribute to the compound's properties.

1,1-Dioxide moiety

A group consisting of two oxygen atoms bonded to a single carbon atom, which can affect the compound's polarity, solubility, and reactivity.

Potential applications

Due to its unique chemical structure, 2-[2-(4-chlorophenyl)-2-oxoethyl]-1,2-benzisothiazol-3(2H)-one 1,1-dioxide may have potential uses in various fields, such as pharmaceuticals, agriculture, and materials science.

Need for further research

To fully understand the properties and potential uses of this chemical, additional research and analysis are required. This may include studying its chemical reactivity, stability, solubility, and biological activity, as well as exploring its potential applications in different industries.

Upstream product

• 58518-76-6 ((1-(4-chlorophenyl)vinyl)oxy)trimethylsilane 
• 99-91-2 para-chloroacetophenone 
• 81-07-2 saccharin 
• 128-44-9 saccharin sodium salt 
• 536-38-9 4-chlorobenzoylmethyl bromide 

Downstream Products

• 1369377-41-2 4-[3-(4-chlorophenyl)-4-methyl-5,5-dioxidopyrazolo[4,3-c][1,2]benzothiazin-1(4H)-yl]benzenesulfonamide 
• 1369377-42-3 3-(4-chlorophenyl)-4-methyl-1-(4-nitrophenyl)-1,4-dihydropyrazolo[4,3-c][1,2]benzothiazine 5,5-dioxide 
• 1369377-43-4 N-{4-[3-(4-chlorophenyl)-4-methyl-5,5-dioxidopyrazolo[4,3-c][1,2]benzothiazin-1(4H)-yl]phenyl}methanesulfonamide 
• 1369377-26-3 (4-chlorophenyl)(4-hydroxy-1,1-dioxido-2H-1,2-benzothiazin-3-yl)methanone 
• 1369377-27-4 3-(4-chlorophenyl)-1-phenyl-1,4-dihydropyrazolo[4,3-c][1,2]benzothiazine 5,5-dioxide 
• 1369377-28-5 3-(4-chlorophenyl)-1-(3-fluorophenyl)-1,4-dihydropyrazolo[4,3-c][1,2]benzothiazine 5,5-dioxide 
• 1369377-29-6 3-(4-chlorophenyl)-1-(4-fluorophenyl)-1,4-dihydropyrazolo[4,3-c][1,2]benzothiazine 5,5-dioxide 
• 1369377-30-9 3-(4-chlorophenyl)-1-[3-(trifluoromethyl)phenyl]-1,4-dihydropyrazolo[4,3-c][1,2]benzothiazine 5,5-dioxide 
• 1369377-31-0 3-(4-chlorophenyl)-1-[4-(trifluoromethyl)phenyl]-1,4-dihydropyrazolo[4,3-c][1,2]benzothiazine 5,5-dioxide 
• 1369377-32-1 4-[3-(4-chlorophenyl)-5,5-dioxidopyrazolo[4,3-c][1,2]benzothiazin-1(4H)-yl]benzenesulfonamide 
• 1369377-33-2 3-(4-chlorophenyl)-1-(4-nitrophenyl)-1,4-dihydropyrazolo[4,3-c][1,2]benzothiazine 5,5-dioxide 
• 1242050-92-5 (4-hydroxy-2-methyl-1,1-dioxo-2H-benzo[e][1,2]thiazin-3-yl)(4-chlorophenyl)methanone 
• 1369377-40-1 3-(4-chlorophenyl)-4-methyl-1-[4-(trifluoromethyl)phenyl]-1,4-dihydropyrazolo[4,3-c][1,2]benzothiazine 5,5-dioxide 
• 1369377-39-8 3-(4-chlorophenyl)-4-methyl-1-[3-(trifluoromethyl)phenyl]-1,4-dihydropyrazolo[4,3-c][1,2]benzothiazine 5,5-dioxide 

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