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

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

• 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 
• 109-72-8 n-butyllithium 
• 14674-38-5 N-(4-methoxybenzylidene)-p-toluenesulfonamide 

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

Triiodide-Mediated δ-Amination of Secondary C?H Bonds

The Cδ?H amination of unactivated, secondary C?H bonds to form a broad range of functionalized pyrrolidines has been developed by a triiodide (I3?)-mediated strategy. By in situ 1) oxidation of sodium iodide and 2) sequestration of the transiently generated iodine (I2) as I3?, this approach precludes undesired I2-mediated decomposition which can otherwise limit synthetic utility to only weak C(sp3)?H bonds. The mechanism of this triiodide-mediated cyclization of unbiased, secondary C(sp3)?H bonds, by either thermal or photolytic initiation, is supported by NMR and UV/Vis data, as well as intercepted intermediates.

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.

Removal of Toluene-p-sulphonyl Groups from Sulphonamides. Part 5. Reactions of Phenylglyoxal Imines and some Tosylimines

Phenylglyoxal anil monomers have been shown to react with several nucleophilic reagents and the structures of the products have been elucidated.Various N-tosylarylimines also react with nucleophiles to give useful products.Phenacylimidates underwent cycloadditions with diphenylketen; such reactions gave complex results with phenacylimines, but the latter reacted with conjugated dienes in the presence of BF3 to give cycloaddition products in good yield.