79807-48-0

Basic information

• Product Name: Benzenesulfonamide, N-[1-(4-methoxyphenyl)pentyl]-4-methyl-
• CAS NO: 79807-48-0
• Molecular Formula: C19H25NO3S
• Molecular Weight: 347.478
• Mol File: 79807-48-0.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Benzenesulfonamide, N-[1-(4-methoxyphenyl)pentyl]-4-methyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenesulfonamide, N-[1-(4-methoxyphenyl)pentyl]-4-methyl-(79807-48-0)
• EPA Substance Registry System: Benzenesulfonamide, N-[1-(4-methoxyphenyl)pentyl]-4-methyl-(79807-48-0)

Safety Data

• Hazardous Substances Data: 79807-48-0(Hazardous Substances Data)

Upstream product

• 109-72-8 n-butyllithium 
• 14674-38-5 N-(4-methoxybenzylidene)-p-toluenesulfonamide 
• 542-69-8 1-iodo-butane 
• 14674-38-5 (E)-N-(4-methoxybenzylidene)-4-methylbenzenesulfonamide 
• 70-55-3 toluene-4-sulfonamide 
• 123-11-5 4-methoxy-benzaldehyde 
• 19523-03-6 1-(4-methoxyphenyl)pentanol 

Relevant articles and documents

Tin-free intermolecular addition of primary alkyls to imines via the dimethylzinc-air radical process

(Chemical Equation Presented) A dimethylzinc-air initiator was applied to the generation of primary alkyl radicals from alkyl iodides. The addition of the generated primary alkyl radicals to N-tosylimines was accelerated by the action of boron trifluoride

Iron-catalyzed N-alkylation using π-activated ethers as electrophiles

A new method for the synthesis of diverse N-alkylation compounds was developed via an iron-catalyzed etheric Csp3-O cleavage with the C-N bond formation in the reaction of π-activated ethers with various nitrogen-based nucleophiles. In addition, the mechanism of this reaction was investigated. The Royal Society of Chemistry 2013.