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.

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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.

Sultam compound and preparation method thereof

The invention provides a sultam compound and a preparation method thereof. The method provided by the invention specifically comprises the following steps: putting a catalyst C, sulfamide B and an oxidant D into an organic solvent, performing a reaction,

Vancomycin-iridium (III) interaction: An unexplored route for enantioselective imine reduction

The chiral structure of antibiotic vancomycin (Van) was exploited as an innovative coordination sphere for the preparation of an IrCp* based hybrid catalysts. We found that Van is able to coordinate iridium (Ir(III)) and the complexation was demonstrated by several analytical techniques such as MALDI-TOF, UV, Circular dichroism (CD), Raman IR, and NMR. The hybrid system so obtained was employed in the Asymmetric Transfer Hydrogenation (ATH) of cyclic imines allowing to obtain a valuable 61% e.e. (R) in the asymmetric reduction of quinaldine 2. The catalytic system exhibited a saturation kinetics with a calculated efficiency of Kcat/KM = 0.688 h?1mM?1