14223-10-0

Basic information

• Product Name: 1-(benzylsulfonyl)-4-methoxybenzene
• Synonyms: 1-(benzylsulfonyl)-4-methoxybenzene
• CAS NO: 14223-10-0
• Molecular Weight: 262.329
• Mol File: 14223-10-0.mol
• Article Data: 22

Chemical Properties

• CAS DataBase Reference: 1-(benzylsulfonyl)-4-methoxybenzene(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(benzylsulfonyl)-4-methoxybenzene(14223-10-0)
• EPA Substance Registry System: 1-(benzylsulfonyl)-4-methoxybenzene(14223-10-0)

Safety Data

• Hazardous Substances Data: 14223-10-0(Hazardous Substances Data)

Upstream product

• 98-68-0 4-methoxy-phenyl-sulphonyl chloride 
• 696-62-8 para-iodoanisole 
• 100-39-0 benzyl bromide 
• 5720-07-0 4-methoxyphenylboronic acid 
• 260783-80-0 N,N,N--trimethyl--1--phenylmethanaminium trifluoromethanesulfonate 
• 1950-68-1 4-methoxybenzenesulfonyl hydrazide 
• 4525-46-6 benzyltrimethylammonium iodide 
• 103-83-3 N,N'-dimethylbenzylamine 
• 6462-50-6 sodium 4-methoxybenzenesulfinate 
• 33397-21-6 tris(4-methoxyphenyl)bismuth 
• 1146-42-5 p-methoxyphenylsulfonothioic phenyl ester 
• 36651-93-1 1-((4-methoxyphenyl)diazenyl)pyrrolidine 
• 74148-29-1 1-((4-methoxyphenyl)diazenyl)piperidine 
• 7203-92-1 1-(p-Methoxyphenyl)-3,3-dimethyltriazene 

Downstream Products

• 494794-56-8 (((4-methoxyphenyl)sulfonyl)methylene)dibenzene 
• 1563174-00-4 C₂₁H₁₈O₃S 

Relevant articles and documents

Nickel(II), copper(II), and cobalt(II) complexes derived from a new unsymmetrical ONS donor schiff base ligand: Synthesis, characterization, crystal structure, and catalytic activities

A series of Ni(II), Cu(II), and Co(II) complexes, ML2, of a new thioether containing ONS donors have been synthesized, where L = deprotonated Schiff base. The analytical, spectral (FTIR,1H NMR, UV–vis), conductivity, and magnetic stu

Synthesis of sulfone derivatives via palladium-catalyzed cross-coupling of benzyl trimethylammonium triflates and sulfonyl hydrazides

A palladium-catalyzed cross-coupling of benzyl trimethylammonium triflates and sulfonyl hydrazides for the synthesis of various benzyl sulfones is reported. This novel protocol shows widespread functional group tolerance, leading to the desired sulfones in moderate to excellent yields.

Cu2O-catalyzed C–S coupling of quaternary ammonium salts and sodium alkane-/arene-sulfinates

A new protocol for the synthesis of (enantioenriched) benzylic sulfones via the Cu2O-catalyzed C–S bond cross coupling of alkane-/arene-sulfinates and (enantioenriched) benzylic quaternary ammonium salts has been developed. The product benzylic sulfones were obtained in good to high yields (75–96%). Chiral arylmethyl sulfones with high enantiomeric excess (90–94% ee) were also synthesized in the presence of Cu2O and 1,1′-bis-(diphenylphosphino)ferrocene (dppf).