4299-23-4

Basic information

• Product Name: 1,2-Benzisothiazol-3(2H)-one, 2-(2-methylphenyl)-
• CAS NO: 4299-23-4
• Molecular Formula: C14H11NOS
• Molecular Weight: 241.313
• Mol File: 4299-23-4.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 1,2-Benzisothiazol-3(2H)-one, 2-(2-methylphenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: 1,2-Benzisothiazol-3(2H)-one, 2-(2-methylphenyl)-(4299-23-4)
• EPA Substance Registry System: 1,2-Benzisothiazol-3(2H)-one, 2-(2-methylphenyl)-(4299-23-4)

Safety Data

• Hazardous Substances Data: 4299-23-4(Hazardous Substances Data)

Usage

Family

Benzisothiazolone

Structure

Contains a heterocyclic ring

Usage

Building block in the synthesis of pharmaceuticals and agrochemicals

Properties

Antimicrobial and antifungal

Applications

Development of new drugs and biocides

Additional uses

Materials science and organic synthesis

Upstream product

• 95-53-4 o-toluidine 
• 3724-10-5 2-(methylthio)benzoic acid 
• 4892-02-8 Methyl thiosalicylate 
• 20054-44-8 N-(2-methyl)phenyl-2-thiosalicylic acid amide 
• 19602-82-5 2,2'-dithiodibenzoic acid dichloride 

Downstream Products

• 177786-30-0 2,2'-disulfanediyl-di-benzoic acid di-o-toluidide 

Relevant articles and documents

Electrochemical synthesis for benzisothiazol-3(2H)-ones by dehydrogenative N[sbnd]S bond formation

Herein, we report an electrochemical method for the synthesis of benzisothiazol-3(2H)-ones from 2-mercaptobenzamides. The electrochemical reaction proceeds through intramolecular N[sbnd]H/S[sbnd]H coupling cyclization reaction by generating H2 as the nonhazardous side product. Moreover, the developed procedure is highly advantageous due to its short reaction time, mild conditions and wide substrate scope without the employment of metal catalyst and exogenous-oxidant.2009 Elsevier Ltd. All rights reserved.

Method for generating benzisothiazolinone compounds by catalyzing oxidization of molecular oxygen in aqueous phase

The invention provides a method for synthesizing benzisothiazolinone compounds by catalyzing oxidization of molecular oxygen in an aqueous phase. A water-soluble transition metal phthalocyanine compound is taken as a catalyst, and a thiosalicylic acid ami

ON BENZISOTHIAZOLONES: A SERIES WITH A WIDE RANGE OF BACTERIOSTATIC AND

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