70188-11-3

Basic information

• Product Name: 2-acetylphenyl 4-methylbenzenesulfonate
• Synonyms: 2-acetylphenyl 4-methylbenzenesulfonate
• CAS NO: 70188-11-3
• Molecular Weight: 290.34
• Mol File: 70188-11-3.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: 2-acetylphenyl 4-methylbenzenesulfonate(CAS DataBase Reference)
• NIST Chemistry Reference: 2-acetylphenyl 4-methylbenzenesulfonate(70188-11-3)
• EPA Substance Registry System: 2-acetylphenyl 4-methylbenzenesulfonate(70188-11-3)

Safety Data

• Hazardous Substances Data: 70188-11-3(Hazardous Substances Data)

Upstream product

• 118-93-4 o-hydroxyacetophenone 
• 98-59-9 p-toluenesulfonyl chloride 

Downstream Products

• 118-93-4 o-hydroxyacetophenone 
• 1111249-52-5 2-(2-methyl-1,3-dioxolan-2-yl)phenyl tosylate 
• 71702-05-1 2-(1-Hydroxyethyl)-phenyl-p-toluolsulfonat 
• 78515-27-2 C₃₀H₂₈O₆S₂ 

Relevant articles and documents

Synthesis, anti-oomycete activity, and SAR studies of paeonol derivatives

Three series of sulfonate derivatives of paeonol were synthesized and screened in?vitro for their anti-oomycete activity against P. capsici, respectively. Among all the compounds, 4m displayed the best promising and pronounced anti-oomycete activity again

Suzuki-Miyaura coupling of aryl sulfonates with arylboronic acids using a morpholine-Pd(OAc)2 catalyst system

We report a new catalyst system, a morpholine-Pd(OAc)2 complex, for Suzuki-Miyaura coupling of aryl tosylates or mesylates with arylboronic acids to give biaryl compounds. The morpholine-Pd(OAc)2 catalyst system is proposed to be a precursor of the catalytically active species in the coupling reaction. Aryl chlorides and aryl triflates can also be used in this coupling reaction. Altogether, 22 biaryl compounds were obtained using this catalyst system. We report a new catalyst system, a morpholine-Pd(OAc) 2 complex, for Suzuki-Miyaura coupling of aryl tosylates or mesylates with arylboronic acids to give biaryl compounds. The morpholine-Pd(OAc) 2 catalyst system is proposed to be a precursor of the catalytically active species in the coupling reaction. Copyright

N-heterocyclic carbene derived Nickel-Pincer complexes: Efficient and applicable catalysts for Suzuki-Miyaura coupling reactions of aryl/alkenyl tosylates and mesylates

Catalytic activities of NHC-derived nickel-pincer complexes for the Suzuki-Miyaura coupling reactions of aryl/alkenyl to- sylates and mesylates are described. In the presence of a catalytic amount of nickelacycle 1a, a wide array of tosylates and mesylates reacted with several aryl- and alkenylboronic acids to afford the coupling products, generally in high yields. Fine tuning of the reaction conditions for each class of electrophiles was achieved only by choosing the appropriate reaction medium (DME for tosylates, dioxane for mesylates).