16191-87-0

Basic information

• Product Name: 4-METHOXYPHENYL VINYLSULPHONE
• Synonyms: p-Anisyl vinyl sulfone;p-Methoxyphenylvinyl sulfone;4-METHOXYPHENYL VINYLSULPHONE
• CAS NO: 16191-87-0
• Molecular Formula: C₉H₁₀O₃S
• Molecular Weight: 198.24
• Mol File: 16191-87-0.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 352.3±34.0 °C(Predicted)
• Appearance: /
• Density: 1.188±0.06 g/cm3(Predicted)
• CAS DataBase Reference: 4-METHOXYPHENYL VINYLSULPHONE(CAS DataBase Reference)
• NIST Chemistry Reference: 4-METHOXYPHENYL VINYLSULPHONE(16191-87-0)
• EPA Substance Registry System: 4-METHOXYPHENYL VINYLSULPHONE(16191-87-0)

Safety Data

• Hazardous Substances Data: 16191-87-0(Hazardous Substances Data)

Upstream product

• 16191-81-4 1-(2-chloroethylsulfonyl)-4-methoxybenzene 
• 5535-48-8 PVS 
• 557780-43-5 4-methoxy-N-morpholinobenzenesulfonamide 
• 106-93-4 ethylene dibromide 
• 16411-17-9 (4-methoxyphenyl)(vinyl)sulfane 
• 35848-00-1 1-[(4-methoxyphenyl)-sulfonyl]ethan-2-ol 
• 124-63-0 methanesulfonyl chloride 
• 20761-70-0 1-(2-chloro-ethylsulfanyl)-4-methoxy-benzene 

Downstream Products

• 62021-92-5 1-(2-tert-Butylperoxy-ethanesulfonyl)-4-methoxy-benzene 
• 885052-39-1 5-ethenesulfonyl-2-methoxybenzenesulfonyl chloride 
• 16191-93-8 N-<2-(4-Methoxy-phenylsulfonyl)-aethyl>-tert-butylamin 
• 62022-01-9 Bis-<2-(p-methoxyphenylsulfon)-aethyl>-peroxid 
• 62021-93-6 1-Methoxy-4-[2-(1-methyl-1-phenyl-ethylperoxy)-ethanesulfonyl]-benzene 
• 128176-22-7 C₁₈H₂₀O₆S₂ 
• 69967-36-8 4-[2-(4-methoxy-benzenesulfonyl)-ethyl]-morpholine 

Relevant articles and documents

A four-component reaction of aryldiazonium tetrafluoroborates, sulfur dioxide, 1,2-dibromoethane, and hydrazines

A four-component reaction of aryldiazonium tetrafluoroborates, sulfur dioxide, 1,2-dibromoethane, and hydrazines under metal-free conditions is described, providing a novel and efficient approach to 2-arylsulfonyl hydrazones. This transformation proceeds

Diastereoselective Monofluorocyclopropanation Using Fluoromethylsulfonium Salts

Diarylfluoromethylsulfonium salts, alternatives to freons or advanced fluorinated building blocks, are bench stable and easy-to-use sources of direct fluoromethylene (:CHF) transfer to alkenes. These salts enabled development of a trans-selective monofluorinated Johnson-Corey-Chaykovsky reaction with vinyl sulfones or vinyl sulfonamides to access synthetically challenging monofluorocyclopropane scaffolds. The described method offers rapid access to monofluorinated cyclopropane building blocks with further functionalization opportunities to deliver more complex synthetic targets diastereoselectively.

BISSULFONAMIDE COMPOUNDS AS AGONISTS OF GALR1, COMPOSITIONS, AND METHODS OF USE

Embodiments of the present invention provide bissulfonamide compounds that are agonists of GalR1. The present invention further provides compositions comprising bissulfonamide compounds that are agonists of GalR1, and methods of use of such compounds and compositions.