5697-20-1

Usage

InChI:InChI=1/C7H7NOS/c8-7(9)5-3-1-2-4-6(5)10/h1-4,10H,(H2,8,9)

Upstream product

• 2527-57-3 2,2'-dithiobisbenzamide 
• 15570-18-0 phenyl o-mercaptobenzoate 
• 201230-82-2 carbon monoxide 
• 52370-18-0 2-allylsulfanyl-benzamide 
• 2634-33-5 1,2-benzisothiazolin-3-one 
• 64-19-7 acetic acid 
• 7647-01-0 hydrogenchloride 
• 609-66-5 2-chlorobenzamide 
• 119-80-2 2,2'-dithiobenzoic acid 

Downstream Products

• 68463-76-3 2-propionylmercapto-benzoic acid amide 
• 408313-11-1 2-phenyl-2,3-dihydro-benzo[e][1,3]thiazin-4-one 
• 68463-75-2 2-acetylsulfanyl-benzoic acid amide 
• 90564-09-3 (2-carbamoyl-phenylsulfanyl)-acetic acid 
• 114863-49-9 2-(tetra-O-acetyl-β-D-glucopyranosylmercapto)-benzoic acid amide 
• 100370-23-8 2-(2-propoxy-ethylsulfanyl)-benzoic acid amide 
• 2527-57-3 2,2'-dithiobisbenzamide 
• 20054-38-0 S-Aethoxycarbonyl-2-mercapto-benzamid 
• 63223-54-1 2-(3-hydroxy-4-methoxy-phenyl)-2,3-dihydro-benzo[e][1,3]thiazin-4-one 
• 91089-60-0 2-(3-chloro-propyl)-2,3-dihydro-benzo[e][1,3]thiazin-4-one 
• 67839-42-3 [4-(4-oxo-3,4-dihydro-2H-benzo[e][1,3]thiazin-2-yl)-phenoxy]-acetic acid ethyl ester 
• 93301-30-5 2-methyl-2-phenyl-4-oxo-2,3-dihydro-1,3-benzothiazine 
• 92789-12-3 <2-Carbamoyl-phenylmercapto>-essigsaeure-butyl-amid 
• 92436-27-6 (2-Carbamoyl-phenylmercapto)-essigsaeure-(2,4-dichlor-anilid) 

Relevant academic research and scientific papers

PROCESS FOR PREPARING 1,2-BENZOISOTHIAZOLIN-3-ONES

Sodium sulfide hydrate is at least partially dehydrated by heating with N-methyl 2-pyrrolidone. 2-Chlorobenzamide is added to the mixture which is heated further. The mixture is cooled and treated with aqueous hydrogen peroxide to give the sodium salt of 1,2-benzisothiazolin-3-one in good yield. Acidification if desired gives rise to the free 1,2-benzisothiazolin-3-one.

PROCESS FOR PREPARING 1,2-BENZOISOTHIAZOLINE-3-ONE

Sodium sulfide hydrate is at least partially dehydrated by heating with N-methyl 2-pyrrolidone. 2-chlorobenzamide is added to the mixture which is heated further. The mixture is cooled and treated with aqueous hydrogen peroxide to give the sodium salt of 1,2-benzoisothiazoline-3-one in good yield. Acidification if desired gives rise to the free 1,2-benzoisothiazoline-3-one.

The Stereochemistry of Organometallic Compounds. XLIV* Rhodium-Catalysed Hydroformylation of Some Alkenylthio Aromatic Compounds

Rhodium-catalysed reactions of o-[(allyl and butenyl)thio] benzonitriles and benzamides with H2/CO give quantitative yields of aldehydes whereas the corresponding benzylamines give only polymeric material. The results are compared with reactions of the analogous alkenylamines and alkenyloxy compounds.