55660-68-9

Basic information

• Product Name: 4-acetylphenyl 4-nitrobenzenesulfonate
• CAS NO: 55660-68-9
• Molecular Formula: C₁₄H₁₁NO₆S
• Molecular Weight: 321.3052
• Mol File: 55660-68-9.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 529°C at 760 mmHg
• Flash Point: 273.7°C
• Density: 1.418g/cm³
• Vapor Pressure: 2.83E-11mmHg at 25°C
• Refractive Index: 1.599
• CAS DataBase Reference: 4-acetylphenyl 4-nitrobenzenesulfonate(CAS DataBase Reference)
• NIST Chemistry Reference: 4-acetylphenyl 4-nitrobenzenesulfonate(55660-68-9)
• EPA Substance Registry System: 4-acetylphenyl 4-nitrobenzenesulfonate(55660-68-9)

Safety Data

• Hazardous Substances Data: 55660-68-9(Hazardous Substances Data)

Upstream product

• 98-74-8 4-Nitrobenzenesulfonyl chloride 
• 99-93-4 4-Hydroxyacetophenone 
• 261172-44-5 4-acetylphenoxide 
• 30362-87-9 p-Nitrophenyl p-nitrobenzenesulphonate 

Downstream Products

• 1010118-59-8 C₂₁H₁₅NO₆S 
• 1010118-54-3 4'-(p-nitrobenzenesulfonate)-4-hydroxychalcone 
• 20488-43-1 4-acetyl-trans-stilbene 
• 52807-17-7 4-acetyl-2'-methoxybiphenyl 
• 13021-18-6 1-(4'-methoxy-biphenyl-4-yl)-ethanone 
• 92-91-1 biphenyl-4-acetaldehyde 
• 261172-44-5 4-acetylphenoxide 
• 1032476-43-9 4'-(4-nitrobenzenesulfonyloxy)-4-hydroxychalcone 
• 10537-63-0 1-(4-vinylphenyl)ethanone 
• 99-93-4 4-Hydroxyacetophenone 

Relevant articles and documents

Aryl and heteroaryl nosylates as stable and cheap partners for Suzuki-Miyaura cross-coupling reactions

Aryl and heteroaryl para-nitrophenylsulfonates (nosylates) have been successfully engaged for the first time in Suzuki-Miyaura cross-coupling reactions with various aryl or vinylboronic acids (48-98%, 12 examples). The best catalyst/ligand combination have been determined to be 2 mol % of palladium acetate (Pd(OAc)2) and 4 mol % of 2-dicyclohexylphosphino-2′,4′,6′-triisopropylbiphenyl (XPhos) using K3PO4 as base, in tetrahydrofuran at 80 °C. These new reaction conditions notably provide a direct and very efficient access to the natural alkaloid dubamine.

Chemoselective regulation of TREK2 channel: Activation by sulfonate chalcones and inhibition by sulfonamide chalcones

Although it has not been extensively studied, a significant volume of literature suggests that TREK2 will probably turn out to be an important channel in charge of tuning neuronal transmitter and hormone levels. Thus, pharmacological tools which can manip

Evidence for a Single Transition State in the Intermolecular Transfer of a Sulfonyl Group between Oxyanion Donor and Acceptors

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