191085-63-9

Basic information

• Product Name: N-(3-methoxybenzyl)-4-methylbenzenesulfonamide
• Synonyms: N-(3-methoxybenzyl)-4-methylbenzenesulfonamide
• CAS NO: 191085-63-9
• Molecular Weight: 291.371
• Mol File: 191085-63-9.mol
• Article Data: 13

Chemical Properties

• CAS DataBase Reference: N-(3-methoxybenzyl)-4-methylbenzenesulfonamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-(3-methoxybenzyl)-4-methylbenzenesulfonamide(191085-63-9)
• EPA Substance Registry System: N-(3-methoxybenzyl)-4-methylbenzenesulfonamide(191085-63-9)

Safety Data

• Hazardous Substances Data: 191085-63-9(Hazardous Substances Data)

Upstream product

• 6971-51-3 3-methoxybenzyl alcohol 
• 70-55-3 toluene-4-sulfonamide 
• 160955-96-4 N-[1-(3-Methoxy-phenyl)-meth-(E)-ylidene]-4-methyl-benzenesulfonamide 
• 591-31-1 3-methoxy-benzaldehyde 
• 941-55-9 4-toluenesulfonyl azide 
• 1569524-37-3 trifluoro(3-methoxybenzyl)-λ⁴-borane potassium salt 
• 5071-96-5 3-METHOXYBENZYLAMINE 
• 98-59-9 p-toluenesulfonyl chloride 

Downstream Products

• 1372911-55-1 methyl N-tosyl-2-(3-methoxybenzylamino)acetate 
• 1372911-69-7 N-tosyl-1-(3-methoxybenzylamino)-2-methyl-2-propanol 
• 1372911-85-7 N-tosyl-7-methoxy-4,4-dimethyl-1,2,3,4-tetrahydroisoquinoline 
• 1372911-84-6 N-tosyl-5-methoxy-4,4-dimethyl-1,2,3,4-tetrahydroisoquinoline 
• 1431115-72-8 N-[(2E)-4-hydroxy-2-butenyl]-N-(3-methoxybenzyl)-4-methylbenzenesulfonamide 
• 1197916-12-3 9-methoxy-2-methyl-6,7-dihydrodibenzo[d,f][1,2]thiazepine 5,5-dioxide 

Relevant articles and documents

Nickel/Photoredox Dual Catalytic Cross-Coupling of Alkyl and Amidyl Radicals to Construct C(sp3)-N Bonds

The construction of C(sp3)-N bonds via direct radical-radical cross-coupling under benign conditions is a desirable but challenging approach. Herein, the cross-coupling of alkyl and amidyl radicals to build aliphatic C-N bonds in a concise, mild, and oxid

Method for synthesizing N-alkyl sulfonamide in water

The invention discloses a method for synthesizing N-alkyl sulfonamide in water, in particular to a method for synthesizing an N-alkyl sulfonamide derivative from a sulfonamide derivative and alcohol,and a water-soluble iridium complex is adopted to catalyze the reaction of N-alkyl sulfonamide. Compared with the previous synthesis method, the method has the advantages that a reaction equivalent substrate is used in the reaction process, so that raw material waste is avoided; weak base is used, and reaction conditions are mild; non-toxic and harmless pure water is used as a solvent in the reaction, only water is generated as a by-product, the atom reaction economy is high, and the requirement of green chemistry is met.

Visible-light, iodine-promoted formation of n-sulfonyl imines and n-alkylsulfonamides from aldehydes and hypervalent iodine reagents

Alternative synthetic methodology for the direct installation of sulfonamide functionality is a highly desirable goal within the domain of drug discovery and development. The formation of synthetically valuable N-sulfonyl imines from a range of aldehydes,