94266-24-7

Usage

InChI:InChI=1/C8H9NO2S/c1-11-8(10)6-4-2-3-5-7(6)12-9/h2-5H,9H2,1H3

Upstream product

• 4892-02-8 Methyl thiosalicylate 

Downstream Products

• 2634-33-5 1,2-benzisothiazolin-3-one 
• 54856-20-1 N-[2-(methoxycarbonyl)benzenesulfenyl]-1,2-benzisothiazolin-3-one 
• 532931-63-8 N-acetyl-2-methoxycarbonylbenzenesulfenamide 
• 55255-11-3 methyl 2-[N-(p-methoxyphenyl)sulfenamoyl]benzoate 
• 4322-81-0 2-(4-chlorobenzyl)benzo[d]isothiazol-2(3H)-one 
• 130266-79-4 2-(4-methoxybenzyl)-1,2-benzisothiazol-3(2H)-one 
• 2514-36-5 2-benzylbenzo[d]isothiazol-3(2H)-one 
• 658702-70-6 N-[(2-methoxycarbonylbenzene)sulfenyl]benzimidazole 
• 444993-96-8 methyl 2-[N-(p-methylphenyl)sulfenamoyl]benzoate 
• 55255-14-6 N-2-methoxycarbonylphenylthio-2-methoxycarbonylbenzenesulfenamide 
• 532931-54-7 N-(trifluoroacetyl)-2-(methoxycarbonyl)benzenesulfenamide 
• 5459-63-2 bis[2-(methoxycarbonyl)phenyl]disulfide 
• 34757-99-8 methyl 2-(N-phenylsulfenamoyl)benzoate 

Relevant academic research and scientific papers

Synthesis and reaction of N-sulfenylpyrroles

N-Sulfenylpyrroles were synthesized by the condensation of N-unsubstituted sulfenamides with 1,4-dicarbonyl compounds, such as hexane-2,5-dione or 2,5-dimethoxytetrahydrofuran. Primary amines as nucleophiles did not attack to the sulfur atom of the N-S bo

A facile synthesis of 1,2-benzisothiazolin-3-ones from thiosalicylates

Synthesis of 1,2-benzisothiazolin-3-ones by cyclization of 2- sulfenamoylbenzoates, which were prepared from amination of thiosalicylates by hydroxylamine-O-sulfonic acid, was examined. Although treatment of methyl 2-sulfenamoylbenzoate on heating gave unexpected 2-(2- methoxycarbonylphenylthio)-1,2-benzisothiazolin-3-one, the treatment with base at room temperature afforded 1,2-benzisothiazolin-3-one in a good yield.