25917-49-1

Basic information

• Product Name: Ethanone, 1-(4-chlorophenyl)-2-[[(4-methylphenyl)sulfonyl]oxy]-
• CAS NO: 25917-49-1
• Molecular Formula: C15H13ClO4S
• Molecular Weight: 324.785
• Mol File: 25917-49-1.mol
• Article Data: 51

Chemical Properties

• CAS DataBase Reference: Ethanone, 1-(4-chlorophenyl)-2-[[(4-methylphenyl)sulfonyl]oxy]-(CAS DataBase Reference)
• NIST Chemistry Reference: Ethanone, 1-(4-chlorophenyl)-2-[[(4-methylphenyl)sulfonyl]oxy]-(25917-49-1)
• EPA Substance Registry System: Ethanone, 1-(4-chlorophenyl)-2-[[(4-methylphenyl)sulfonyl]oxy]-(25917-49-1)

Safety Data

• Hazardous Substances Data: 25917-49-1(Hazardous Substances Data)

Upstream product

• 104-15-4 toluene-4-sulfonic acid 
• 74-11-3 para-chlorobenzoic acid 
• 3391-10-4 1-(p-chlorophenyl)ethyl alcohol 
• 99-91-2 para-chloroacetophenone 
• 73177-96-5 <(hydroxy)(tosyloxy)iodo>-p-toluene 
• 27126-76-7 [hydroxy(tosyloxy)iodo]benzene 
• 16836-95-6 silver(I) 4-methylbenzenesulfonate 
• 536-38-9 4-chlorobenzoylmethyl bromide 

Downstream Products

• 141421-05-8 3-(4-Chloro-phenyl)-5,6-dihydro-imidazo[2,1-b]thiazole; compound with toluene-4-sulfonic acid 
• 2104-00-9 4-(4'-chloro)-phenyl-Δ-4-thiazolene-2-thione 
• 7178-24-7 2-(4-chlorophenyl)-7-methoxyimidazo[2,1-b]benzothiazole 
• 7025-34-5 2-(4-chlorophenyl)-7-methylimidazo[2,1-b]benzothiazole 
• 7025-32-3 2-(4-chlorophenyl)benzo[d]imidazo[2,1-b][1,3]thiazole 
• 17286-63-4 2-(4-chlorophenyl)quinoxaline 
• 133116-39-9 3-(4-chlorophenyl)-4H-furo[3,2-c]chromen-4-one 
• 1345694-83-8 C₁₆H₁₇ClO₃ 
• 871707-72-1 C₁₅H₁₀Cl₂N₂ 
• 429656-76-8 C₁₇H₁₁ClN₂S 
• 1294503-38-0 C₁₄H₁₀ClN₃ 
• 40046-26-2 p-Chlorophenacyl isothiocyanate 

Relevant articles and documents

Organic reactions in ionic liquids: Ionic liquid-accelerated cyclocondensation of α-tosyloxyketones with 2-aminopyridine

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Diastereoselective Alkene Hydroesterification Enabling the Synthesis of Chiral Fused Bicyclic Lactones

Palladium-catalysed diastereoselective hydroesterification of alkenes assisted by the coordinative hydroxyl group in the substrate afforded a variety of chiral γ-butyrolactones bearing two stereocenters. Employing the carbonylation-lactonization products as the key intermediates, the route from the alkenes with single chiral center to chiral THF-fused bicyclic γ-lactones containing three stereocenters was developed.

A convenient [hydroxy(tosyloxy)iodo]benzene-mediated one-pot synthesis of 2-arylimidazo[2,1-b[benzothiazoles

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