84108-98-5

Basic information

• Product Name: 2,3-Dihydro-3-methyl-1,2-benzisothiazole 1,1-Dioxide
• Synonyms: 2,3-Dihydro-3-methyl-1,2-benzisothiazole 1,1-Dioxide;3-Methyl-2,3-dihydrobenzo[d]isothiazole 1,1-dioxide
• CAS NO: 84108-98-5
• Molecular Formula: C₈H₉NO₂S
• Molecular Weight: 183
• Mol File: 84108-98-5.mol
• Article Data: 17

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2,3-Dihydro-3-methyl-1,2-benzisothiazole 1,1-Dioxide(CAS DataBase Reference)
• NIST Chemistry Reference: 2,3-Dihydro-3-methyl-1,2-benzisothiazole 1,1-Dioxide(84108-98-5)
• EPA Substance Registry System: 2,3-Dihydro-3-methyl-1,2-benzisothiazole 1,1-Dioxide(84108-98-5)

Safety Data

• Hazardous Substances Data: 84108-98-5(Hazardous Substances Data)

Usage

Type of compound

Fungicide

Usage

Protects crops from fungal diseases (e.g. smuts, bunts)

Mode of action

Inhibits growth of fungal cells and interferes with energy production

Application method

Typically applied to seeds before planting and absorbed by the seed

Mammalian toxicity

Low

Agricultural uses

Protects crops such as wheat, barley, and rice

Ongoing research

To develop alternative, more environmentally friendly fungicides.

Upstream product

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• 1351416-37-9 2-ethylbenzenesulfonyl azide 
• 958752-88-0 C₁₄H₁₄BrNO₃S 
• 849056-66-2 C₁₁H₁₀BrNO₃S 
• 2905-25-1 o-bromobenzenesulfonyl chloride 
• 91-63-4 2-methylquinoline 
• 4721-98-6 6,7-dimethoxy-1-methyl-3,4-dihydroisoquinoline 
• 81-07-2 saccharin 
• 1973-22-4 1-bromo-2-ethylbenzene 
• 34586-43-1 2-ethylbenzenesulfonyl chloride 

Relevant articles and documents

Efficient visible-light photocatalytic aerobic oxidation of cyclic sulfamides to imines

A highly efficient photocatalytic aerobic oxidation of cyclic sulfamides to synthesize cyclic N-sulfonyl imines with Ir(ppy)2(dtbpy)PF6 as photocatalyst is reported. These environmentally friendly transformations exihibit good to excellent isolated yields and good generality with respect to both five-membered and six-membered cyclic sulfamides.

Reductions of Imines Using Zirconocene Chloride Hydride

Herein, we describe the fast, chemoselective, and clean reduction of imines with zirconocene chloride hydride. The reaction works well on aromatic and enolizable aliphatic aldimines, as well as ketimines. A range of N-protecting groups and various functio

Cobalt-Catalyzed Transfer Hydrogenation of α-Ketoesters and N-Cyclicsulfonylimides Using H2O as Hydrogen Source

A Co-catalyzed effective transfer hydrogenation of various α-ketoesters and N-cyclicsulfonylimides by safe and environmentally benign H2O as hydrogen source is described. The reaction used easily available and easy to handle zinc metal as a reductant. Interestingly, the catalytic system does not require ligand for reduction of N-cyclicsulfonylimides. (Figure presented.).