1363131-17-2

Basic information

• Product Name: N,N-bis((E)-3-(4-methoxyphenyl)allyl)-4-methylbenzenesulfonamide
• Synonyms: N,N-bis((E)-3-(4-methoxyphenyl)allyl)-4-methylbenzenesulfonamide
• CAS NO: 1363131-17-2
• Molecular Weight: 463.598
• Mol File: 1363131-17-2.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: N,N-bis((E)-3-(4-methoxyphenyl)allyl)-4-methylbenzenesulfonamide(CAS DataBase Reference)
• NIST Chemistry Reference: N,N-bis((E)-3-(4-methoxyphenyl)allyl)-4-methylbenzenesulfonamide(1363131-17-2)
• EPA Substance Registry System: N,N-bis((E)-3-(4-methoxyphenyl)allyl)-4-methylbenzenesulfonamide(1363131-17-2)

Safety Data

• Hazardous Substances Data: 1363131-17-2(Hazardous Substances Data)

Upstream product

• 90841-43-3 (E)-4-methoxycinnamyl bromide 
• 1000979-69-0 4-methyl-N-[(2E)-3-(4-methoxyphenyl)-2-propenyl]benzenesulfonamide 

Relevant articles and documents

Endoperoxide synthesis by photocatalytic aerobic [2 + 2 + 2] cycloadditions

Structurally novel endoperoxides can be sythesized by the photocatalytic cyclotrimerization of bis(styrene) substrates with molecular oxygen. The optimal catalyst for this process is Ru(bpz)32+, which is a markedly more efficient catalyst for these photooxygention reactions than conventional organic photosensitizers. The 1,2-dioxolane products are amenable to synthetic manipulation and can be easily processed to 1,4-diols and γ-hydroxyketones. An initial screen of the biological activity of these compounds reveals promising inhibition of cancer cell growth.