4284-48-4

Basic information

• Product Name: Methanesulfonamide, N-(4-methoxyphenyl)-
• CAS NO: 4284-48-4
• Molecular Formula: C8H11NO3S
• Molecular Weight: 201.246
• Mol File: 4284-48-4.mol
• Article Data: 33

Chemical Properties

• CAS DataBase Reference: Methanesulfonamide, N-(4-methoxyphenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Methanesulfonamide, N-(4-methoxyphenyl)-(4284-48-4)
• EPA Substance Registry System: Methanesulfonamide, N-(4-methoxyphenyl)-(4284-48-4)

Safety Data

• Hazardous Substances Data: 4284-48-4(Hazardous Substances Data)

Upstream product

• 104-94-9 4-methoxy-aniline 
• 124-63-0 methanesulfonyl chloride 
• 5720-07-0 4-methoxyphenylboronic acid 
• 624-90-8 Methanesulfonyl azide 
• 67-68-5 dimethyl sulfoxide 
• 3144-09-0 methanesulfonamide 
• 696-62-8 para-iodoanisole 
• 104-92-7 1-bromo-4-methoxy-benzene 
• 123-11-5 4-methoxy-benzaldehyde 
• 54769-22-1 1-methanesulfonyloxy-1,2,3-benzotriazole 
• 7143-01-3 Methanesulfonic anhydride 

Downstream Products

• 86662-01-3 N-(4-methoxy-2-nitrophenyl)methanesulfonamide 
• 116599-13-4 methanesulfonic acid-(2,5-dichloro-4-methoxy-anilide) 
• 118926-53-7 methanesulfonic acid-(2,5-dibromo-4-methoxy-anilide) 
• 22729-87-9 N-(4-Methoxy-phenyl)-N-(1,1,2,2-tetrachloro-2-fluoro-ethylsulfanyl)-methanesulfonamide 
• 108297-28-5 N-(4-Methoxy-2-pyrrolidin-1-ylmethyl-phenyl)-methanesulfonamide 
• 88131-58-2 N-(3,3-Diethoxy-propyl)-N-(4-methoxy-phenyl)-methanesulfonamide 
• 88156-68-7 N-(2,2-Diethoxy-ethyl)-N-(4-methoxy-phenyl)-methanesulfonamide 
• 333383-72-5 N-(4-methoxy-phenyl)-N-(3-oxo-propyl)-methanesulfonamide 
• 23004-83-3 N-(4-methoxyphenyl)-N-(prop-2-en-1-yl)methanesulfonamide 
• 877082-24-1 dithiocarbonic acid (5-chloro-1-{[methanesulfonyl-(4-methoxyphenyl)-amino]-methyl}-4-oxo-pentyl) ester ethyl ester 
• 5263-87-6 6-methoxy quinoline 
• 935-50-2 4,4-dimethoxycyclohexa-2,5-dienone 
• 1006-94-6 5-methoxylindole 
• 5350-56-1 4-amino-1-methoxy-3,5-dinitrobenzene 

Relevant articles and documents

Electrosynthesis of sulfonamides from DMSO and amines under mild conditions

With DMSO as the solvent and the precursor of a -SO2Me unit at room temperature, a novel electrochemical oxidization and amination of DMSO with amines was developed for the synthesis of sulfonamides. Our investigations reveal that this transformation may involve a radical process and an electrochemical oxidization of DMSO.

Meta Selective C-H Borylation of Sterically Biased and Unbiased Substrates Directed by Electrostatic Interaction

An electrostatically directed meta borylation of sterically biased and unbiased substrates is described. The borylation follows an electrostatic interaction between the partially positive and negative charges between the ligand and substrate. With this strategy, it has been demonstrated that a wide number of challenging substrates, especially 4-substituted substrates, can selectively be borylated at the meta position. Moreover, unsubstituted substrates also displayed excellent meta selectivity. The reaction employs a bench-stable ligand and proceeds at a milder temperature, precluding the need to synthesize a bulky and sophisticated ligand/template.

Nitrogen-Bridged, Natural Product Like Octahydrobenzofurans and Octahydroindoles: Scope and Mechanism of Bridge-Forming Reductive Amination via Caged Heteroadamantanes

The biological significance of sp3-rich synthetic scaffolds with natural product like features yet distinct global frameworks is being increasingly recognized in medicinal chemistry and biochemistry. Taking inspiration from the vast array of bi