78315-86-3

Basic information

• Product Name: 1-hydroxy-4-(2-nitrophenylthio)naphthalene
• Synonyms: 1-hydroxy-4-(2-nitrophenylthio)naphthalene
• CAS NO: 78315-86-3
• Molecular Weight: 297.334
• Mol File: 78315-86-3.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 1-hydroxy-4-(2-nitrophenylthio)naphthalene(CAS DataBase Reference)
• NIST Chemistry Reference: 1-hydroxy-4-(2-nitrophenylthio)naphthalene(78315-86-3)
• EPA Substance Registry System: 1-hydroxy-4-(2-nitrophenylthio)naphthalene(78315-86-3)

Safety Data

• Hazardous Substances Data: 78315-86-3(Hazardous Substances Data)

Upstream product

• 90-15-3 α-naphthol 
• 7669-54-7 2-nitrobenzenesulfenyl chloride 
• 22024-99-3 2-nitrobenzenesulfenyl bromide 
• 22057-44-9 1-(benzylsulfanyl)-2-nitrobenzene 
• 1155-00-6 bis(2-nitrophenyl)disulfide 
• 88-73-3 2-Chloronitrobenzene 

Relevant articles and documents

TBATB mediated debenzylative cross-coupling of aryl benzyl sulfides with electron rich compounds: Synthesis of diaryl sulfides

An efficient TBATB mediated debenzylative cross coupling of aryl benzyl sulfides with electron rich compounds provides diaryl sulfides in moderate to excellent yield. The salient features of the present protocol are simplicity, high efficiency and compati

Directed Reactions of C-Sulfenyl Halides with 1-Hydroxynaphthalene Derivatives

C-Sulfenyl chlorides react with 1-hydroxynaphthalene derivatives in nitrobenzene with the formation of sulfenylation products sulfenylation. Under the same conditions C-sulfenyl bromides furnish the products of bromination. In the presence of potassium perchlorate the reactions occurs place also in dioxane and acetonitrile with retention of different in reactivity patterns of isostructural chlorides and bromides. In the reaction with 1-hydroxynaphthalene 2-nitro- and 2,4-dinitrobenzenesulfenylbromides both afford the bromination and sulfenylation products in unsimilar ratios.