58297-34-0

Basic information

• Product Name: Ethanone, 1-[3-[[(4-methylphenyl)sulfonyl]oxy]phenyl]-
• CAS NO: 58297-34-0
• Molecular Formula: C15H14O4S
• Molecular Weight: 290.34
• Mol File: 58297-34-0.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: Ethanone, 1-[3-[[(4-methylphenyl)sulfonyl]oxy]phenyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: Ethanone, 1-[3-[[(4-methylphenyl)sulfonyl]oxy]phenyl]-(58297-34-0)
• EPA Substance Registry System: Ethanone, 1-[3-[[(4-methylphenyl)sulfonyl]oxy]phenyl]-(58297-34-0)

Safety Data

• Hazardous Substances Data: 58297-34-0(Hazardous Substances Data)

Upstream product

• 121-71-1 3-Hydroxyacetophenone 
• 98-59-9 p-toluenesulfonyl chloride 

Downstream Products

• 59695-23-7 1-(3-morpholinophenyl)ethan-1-one 
• 893734-63-9 1-(3'-methoxy[1,1'-biphenyl]-3-yl)ethan-1-one 
• 1078710-19-6 1-{2'-(4,5-dihydrooxazol-2-yl)-3'-methyl-[1,1'-biphenyl]-3-yl}ethan-1-one 
• 182169-63-7 3-acetyl-4'-methoxybiphenyl 
• 214360-49-3 1-[3-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-phenyl]-ethanone 
• 1067883-71-9 3'-(2-naphthyl)acetophenone 
• 23699-65-2 1-(3-(phenylamino)phenyl)ethan-1-one 

Relevant articles and documents

Chromatography-Free and Eco-Friendly Synthesis of Aryl Tosylates and Mesylates

Two chromatography-free and eco-friendly protocols have been developed to synthesize aryl tosylates and mesylates by the tosylation and mesylation of the corresponding hydroxyarenes, respectively. These protocols are superior to other known ones regarding

Palladium-catalyzed borylation of aryl mesylates and tosylates and their applications in one-pot sequential suzuki-miyaura biaryl synthesis

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Suzuki-Miyaura coupling of aryl tosylates catalyzed by an array of indolyl phosphine-palladium catalysts

A family of indolyl phosphine ligands was applied to Suzuki-Miyaura cross-coupling of aryl tosylates. Catalyst loading can be reduced to 0.2 mol % for coupling of nonactivated aryl tosylate. A challenging example for room temperature coupling is realized. The scope of this highly active Pd/L2 system can be extended to other boron nucleophiles, including trifluoroborate salts and boronate esters. The ligand structural comparisons toward the reactivity in tosylate couplings are also described.