68340-48-7

Basic information

• Product Name: sodium 4-chlorodithiobenzoate
• Synonyms: sodium 4-chlorodithiobenzoate
• CAS NO: 68340-48-7
• Molecular Weight: 210.684
• Mol File: 68340-48-7.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: sodium 4-chlorodithiobenzoate(CAS DataBase Reference)
• NIST Chemistry Reference: sodium 4-chlorodithiobenzoate(68340-48-7)
• EPA Substance Registry System: sodium 4-chlorodithiobenzoate(68340-48-7)

Safety Data

• Hazardous Substances Data: 68340-48-7(Hazardous Substances Data)

Upstream product

• 5216-25-1 4-chlorotrichloromethylbenzene 

Downstream Products

• 80031-14-7 N-<4-(chloro)thiobenzoylthio>succinimide 
• 80031-21-6 4-Chloro-dithiobenzoic acid 1,3-dioxo-1,3-dihydro-isoindol-2-yl ester 
• 80047-64-9 Propionic 4-chlorothiobenzoic thioanhydride 
• 128204-62-6 N-(4-Chloro-thiobenzoylsulfanyl)-4-methoxy-benzamide 
• 128204-61-5 Dodecanoic acid (4-chloro-thiobenzoylsulfanyl)-amide 
• 128204-60-4 4-Chloro-N-(4-chloro-thiobenzoylsulfanyl)-benzamide 
• 2227-72-7 2-(4′-chlorophenyl)-4-phenylthiazole 
• 100008-77-3 4-Chloro-dithiobenzoic acid 2-oxo-2-phenyl-ethyl ester 
• 97346-62-8 selenium bis<4-(chloro)dithiobenzoate> 
• 35124-72-2 S-(p-Chlorothiobenzoyl)-hydrosulfamin 
• 64586-16-9 Acetic 4-chlorothiobenzoic thioanhydride 

Relevant articles and documents

Preparation and reactions of 5-Aryl-1,4,2-dithiazolium salts

S-Thioaroylsulfenamides (ArCSSNH2), formed by reaction of ArCSS-Na+ with hydroxylamine-O-sulfonic acid, were aroylated or acylated to give N-aroyl- or N-acyl-S-thioaroylsulfenamides, respectively, which were then cyclized with dehydration to afford 3-substituted 5-aryl-1,4,2-dithiazolium salts. The behavior of 3,5-diphenyl-1,4,2-dithiazolium Perchlorate toward nucleophiles such as active methylene and amino compounds was studied systematically. The reaction can be classified into two cases depending on fission modes of initial adducts, i.e., ring opening-ring closure reaction (Path B) and fragmentation of dithiazole ring (Path C), and in some cases the initial adducts were isolated.