1399347-20-6

Basic information

• Product Name: N-allyl-1-(3,4,5-trimethoxyphenyl)-4-(4-methoxyphenyl)-N-methylbut-3-yn-2-amine
• Synonyms: N-allyl-1-(3,4,5-trimethoxyphenyl)-4-(4-methoxyphenyl)-N-methylbut-3-yn-2-amine
• CAS NO: 1399347-20-6
• Molecular Weight: 395.499
• Mol File: 1399347-20-6.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: N-allyl-1-(3,4,5-trimethoxyphenyl)-4-(4-methoxyphenyl)-N-methylbut-3-yn-2-amine(CAS DataBase Reference)
• NIST Chemistry Reference: N-allyl-1-(3,4,5-trimethoxyphenyl)-4-(4-methoxyphenyl)-N-methylbut-3-yn-2-amine(1399347-20-6)
• EPA Substance Registry System: N-allyl-1-(3,4,5-trimethoxyphenyl)-4-(4-methoxyphenyl)-N-methylbut-3-yn-2-amine(1399347-20-6)

Safety Data

• Hazardous Substances Data: 1399347-20-6(Hazardous Substances Data)

Upstream product

• 182217-53-4 1,2,3-trimethoxy-5-(2-methoxyvinyl)benzene 
• 86-81-7 3,4,5-trimethoxy-benzaldehyde 
• 627-37-2 N-methyl-N-allylamine 
• 5320-31-0 3,4,5-trimethoxyphenylacetaldehyde 
• 768-60-5 4-methoxyphenylacetylen 

Downstream Products

• 1399347-24-0 4-(4-methoxyphenyl)-N-methyl-1-(3,4,5-trimethoxyphenyl)but-3-yn-2-amine 
• 1399347-28-4 C₃₂H₄₃N₃O₈ 
• 1399347-30-8 C₃₁H₄₁N₃O₇ 

Relevant articles and documents

Palladium (II)-catalysed intramolecular C–H functionalizations: Efficient synthesis of kealiinine C and analogues

An efficient palladium-catalysed C–H functionalization sequence has been developed for the synthesis of 2-aminoimidazole alkaloids (Kealiinine C) and its analogues. This protocol proceeds via iodocyclisation of propargylguanidines followed by intramolecul

Synthesis of the reported structures for kealiinines B and C

Syntheses of the reported structures of kealiinines B and C have been executed. An intermolecular electrophile-induced cyclization of a pendant arene on an ene-guanidine affords the tetracyclic, oxidized naphthimidazole cores.