193904-60-8

Basic information

• Product Name: 1,2-Benzisothiazole, 6-ethyl-2,3-dihydro-3-methyl-, 1,1-dioxide (9CI)
• Synonyms: 1,2-Benzisothiazole, 6-ethyl-2,3-dihydro-3-methyl-, 1,1-dioxide (9CI)
• CAS NO: 193904-60-8
• Molecular Formula: C10H13NO2S
• Molecular Weight: 211.28072
• Product Categories: ALCOHOL
• Mol File: 193904-60-8.mol
• Article Data: 5

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1,2-Benzisothiazole, 6-ethyl-2,3-dihydro-3-methyl-, 1,1-dioxide (9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: 1,2-Benzisothiazole, 6-ethyl-2,3-dihydro-3-methyl-, 1,1-dioxide (9CI)(193904-60-8)
• EPA Substance Registry System: 1,2-Benzisothiazole, 6-ethyl-2,3-dihydro-3-methyl-, 1,1-dioxide (9CI)(193904-60-8)

Safety Data

• Hazardous Substances Data: 193904-60-8(Hazardous Substances Data)

Usage

General Description

1,2-Benzisothiazole, 6-ethyl-2,3-dihydro-3-methyl-, 1,1-dioxide (9CI) is a chemical compound with the molecular formula C10H13NO2S. It is also known by the name Ethyl-6-methyl-7-oxo-4,7-dihydrothiazolo[3,2-a]benzimidazol-3-ylideneethanoate. 1,2-Benzisothiazole, 6-ethyl-2,3-dihydro-3-methyl-, 1,1-dioxide (9CI) is a heterocyclic organic compound that contains a thiazole ring fused to a benzene ring. It is used in the manufacturing of pharmaceuticals and agrochemicals due to its versatile chemistry and its ability to act as a building block for various biologically active compounds. 1,2-Benzisothiazole, 6-ethyl-2,3-dihydro-3-methyl-, 1,1-dioxide (9CI) may also have potential applications in materials science and research. Additionally, it is important to handle this chemical with care, as it may pose health and environmental risks if not properly handled and disposed of.

Upstream product

• 193904-59-5 {[(2,5-diethylphenyl)sulfonyl]imino}phenyl-λ³-iodane 
• 91252-29-8 2,5-diethylbenzenesulfonamide 

Relevant articles and documents

Chemoselective, enzymatic C-H bond amination catalyzed by a cytochrome P450 containing an Ir(Me)-PIX cofactor

Cytochrome P450 enzymes have been engineered to catalyze abiological C-H bond amination reactions, but the yields of these reactions have been limited by low chemoselectivity for the amination of C-H bonds over competing reduction of the azide substrate t

Cobalt-catalyzed intramolecular C-H amination with arylsulfonyl azides

(Chemical Equation Presented) Cobalt complexes of porphyrins are effective catalysts for intramolecular C-H amination with arylsulfonyl azides. The cobalt-catalyzed process can proceed efficiently under mild and neutral conditions in low catalyst loading

Rhodium(II)-Catalyzed CH Insertions with imino>phenyl-λ3-iodane

The catalyzed decomposition of imino>phenyl-λ3-iodane (NsN=IPh) resulted in formal insertions into CH bonds, activated by phenyl or vinyl groups, or by O-substituents.Scope and limitations of the reaction were investigated.Yields of up to 84percent were achieved in the most favorable cases.Yields were enhanced by electron-releasing substituents and decreased by steric hindrance.Aziridination competed with allylic insertion with olefinic substrates.The insertion reaction proceeded with retention of configuration.With chiral RhII catalysts, a modest asymmetric induction was observed.A mechanism involving direct insertion by a Rh-complexed nitrene into the CH bond is proposed.