79246-03-0

Basic information

• Product Name: N-(4-methoxybenzyl)benzenesulfonamide
• Synonyms: N-(4-methoxybenzyl)benzenesulfonamide;N-[(4-methoxyphenyl)methyl]benzenesulfonamide
• CAS NO: 79246-03-0
• Molecular Formula: C₁₄H₁₅NO₃S
• Molecular Weight: 277.3388
• Mol File: 79246-03-0.mol
• Article Data: 20

Chemical Properties

• Appearance: /
• CAS DataBase Reference: N-(4-methoxybenzyl)benzenesulfonamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-(4-methoxybenzyl)benzenesulfonamide(79246-03-0)
• EPA Substance Registry System: N-(4-methoxybenzyl)benzenesulfonamide(79246-03-0)

Safety Data

• Hazardous Substances Data: 79246-03-0(Hazardous Substances Data)

Upstream product

• 2393-23-9 4-methoxy-benzylamine 
• 98-09-9 benzenesulfonyl chloride 
• 4358-63-8 phenyl benzenesulfonate 
• 5398-09-4 4-tolyl benzenesulfonate 
• 80-38-6 fenson 
• 3313-84-6 4-nitrophenyl benzenesulfonate 
• 49557-76-8 N-(4-methoxybenzylidene)benzenesulfonamide 
• 623-12-1 4-chloromethoxybenzene 
• 1286686-22-3 potassium phenylsulfonamidomethyltrifluoroborate 
• 98-10-2 benzenesulfonamide 
• 105-13-5 4-Methoxybenzyl alcohol 
• 70-55-3 toluene-4-sulfonamide 
• 123-11-5 4-methoxy-benzaldehyde 
• 873-55-2 sodium benzenesulfonate 

Downstream Products

• 35103-34-5 N-(p-methoxybenzyl)acetamide 
• 98-10-2 benzenesulfonamide 
• 123-11-5 4-methoxy-benzaldehyde 
• 49557-76-8 N-(4-methoxybenzylidene)benzenesulfonamide 

Relevant articles and documents

N -Alkylation of organonitrogen compounds catalyzed by methylene-linked bis-NHC half-sandwich ruthenium complexes

An efficient ruthenium-catalyzed N-alkylation of amines, amides and sulfonamides has been developed employing novel pentamethylcyclopentadienylruthenium(ii) complexes bearing the methylene linked bis(NHC) ligand bis(3-methylimidazol-2-ylidene)methane. The

Synthetic method for catalyzing imine to be reduced into amine

The invention discloses a synthesis method for catalyzing imine to be reduced into amine, wherein the synthesis method is characterized by comprising the following steps: 1, sequentially putting a sulfonyl imine compound and a catalyst I into a reaction bottle according to a reaction molar ratio of 1:0.01 at normal temperature and normal pressure, adding formic acid and a triethylamine solution according to a volume ratio of 5:2, and reacting in a solvent for 1-15 minutes to obtain a reaction product; and 2, after the reaction in the step 1 is finished, sequentially and slowly adding water and ethyl acetate into an obtained reaction product, sufficiently stirring, standing for layering, extracting a separated water layer by using ethyl acetate, combining an extract of ethyl acetate with a separated organic layer, washing by using saturated edible salt water, and drying by using anhydrous sodium sulfate, evaporating to remove the ethyl acetate solvent to obtain a crude product, and separating and purifying by silica gel column chromatography to obtain the amine compound.

Cu-catalyzed aerobic oxidative synthesis of sulfonamides from sulfonyl hydrazides and amines

An environmentally friendly route for sulfonamides has been developed. The oxidative coupling of sulfonyl hydrazides and amines was catalyzed by CuBr2 to produce various sulfonamides with the water and nitrogen gas as byproducts. Preliminary experiments revealed that the sulfonyl radical is likely to be involved in the reaction mechanism.