1535-35-9

Basic information

• Product Name: Benzenesulfenyl chloride, 4-fluoro-
• CAS NO: 1535-35-9
• Molecular Formula: C6H4ClFS
• Molecular Weight: 162.615
• Mol File: 1535-35-9.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: Benzenesulfenyl chloride, 4-fluoro-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenesulfenyl chloride, 4-fluoro-(1535-35-9)
• EPA Substance Registry System: Benzenesulfenyl chloride, 4-fluoro-(1535-35-9)

Safety Data

• Hazardous Substances Data: 1535-35-9(Hazardous Substances Data)

Upstream product

• 2557-77-9 3-fluorothiophenol 
• 75220-74-5 m-fluorobenzenesulfenyl chloride 
• 371-42-6 4-Fluorothiophenol 

Downstream Products

• 3109-53-3 O,O-Diphenyl-S-<4-fluor-phenylmercapto>-dithiophosphat 
• 1544-66-7 O,O-Diaethyl-S-<4-fluor-phenylmercapto>-dithiophosphat 
• 52145-38-7 Methyl-carbamic acid 4-(4-fluoro-phenylsulfanyl)-3,5-dimethyl-phenyl ester 
• 86223-64-5 2,3-Bis(4-methoxyphenyl)-5-(4-fluorphenylthio)-pyrrol 
• 74880-28-7 (1S,2S,3R,4R,6R)-1-Chloromethyl-3-(4-fluoro-phenylsulfanyl)-tricyclo[2.2.1.0^2,6]heptane 
• 333-42-6 thiophosphoric acid O,O'-diethyl ester S-(4-fluorophenyl) ester 

Relevant articles and documents

Unsymmetrical difunctionalization of cyclooctadiene under continuous flow conditions: Expanding the scope of ring opening metathesis polymerization

Functionalized cyclooctenes (FCOEs) are important monomers in ring-opening metathesis polymerization (ROMP). Herein, a new library of disubstituted FCOEs bearing adjacent heteroatoms were synthesized and applied in ROMP. To address the issues associated w

Trichloroisocyanuric acid-promoted thiolation of phosphites by thiols

A simple and convenient method for the synthesis of thiophosphates by coupling of phosphites with thiols under mild conditions has been developed. The reactions were promoted by trichloroisocyanuric acid (TCCA) and were carried out at room temperature in

Oxidation of Electron-Deficient Sulfides to Sulfones Using HOF*CH3CN

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