54429-89-9

Basic information

• Product Name: N-benzyl-3-oxypyridinium betaine
• Synonyms: N-benzyl-3-oxypyridinium betaine
• CAS NO: 54429-89-9
• Molecular Weight: 185.225
• Mol File: 54429-89-9.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: N-benzyl-3-oxypyridinium betaine(CAS DataBase Reference)
• NIST Chemistry Reference: N-benzyl-3-oxypyridinium betaine(54429-89-9)
• EPA Substance Registry System: N-benzyl-3-oxypyridinium betaine(54429-89-9)

Safety Data

• Hazardous Substances Data: 54429-89-9(Hazardous Substances Data)

Upstream product

• 62214-78-2 1-benzyl-3-hydroxypyridin-1-ium bromide 
• 4439-53-6 N-benzyl(furan-2-ylmethyl)amine 
• 100-46-9 benzylamine 
• 109-00-2 3-HYDROXYPYRIDINE 
• 100-39-0 benzyl bromide 
• 100-44-7 benzyl chloride 

Downstream Products

• 863408-70-2 8-benzyl-2-oxo-8-aza-bicyclo[3.2.1]oct-3-ene-6-carbonitrile 
• 1087750-66-0 8-benzyl-6-(phenylsulfonyl)-8-azabicyclo[3.2.1]oct-3-en-2-one 
• 1415146-44-9 C₁₉H₁₇NO₂ 
• 1184103-08-9 12-benzyl-3-(4-chloro-3-methoxyphenyl)-8-(phenylsulfonyl)-2-pyridin-4-yl-7,8,9,10-tetrahydro-6H-7,10-epiminocyclohepta[e]pyrazolo[1,5-a]pyrimidine 
• 1184103-60-3 8-benzyl-3-[(dimethylamino)methylene]-6-(phenylsulfonyl)-8-azabicyclo[3.2.1]octane-2-one 
• 1184103-59-0 8-benzyl-6-(phenylsulfonyl)-8-azabicyclo[3.2.1]octan-2-one 
• 1415146-00-7 C₁₈H₁₅NO 
• 1415146-19-8 C₂₀H₁₉NO₃ 
• 1415146-20-1 C₂₀H₁₉NO₃ 
• 1415146-17-6 C₁₉H₁₇NO₂ 
• 1415146-18-7 C₁₉H₁₇NO₂ 
• 1415146-15-4 C₁₉H₁₇NO₂ 
• 1415146-16-5 C₁₉H₁₇NO₂ 
• 1415146-14-3 C₂₀H₁₉NO₃ 

Relevant articles and documents

Solid-phase synthesis of functionalized tropane derivatives via 1,3-dipolar cycloaddition

1,3-Dipolar cycloaddition of 3-oxidopyridinium betaine to activated olefins on solid-phase leads to resin-bound 8-azabicyclo[3.2.1]octenones which undergo further transformations such as 1,4-addition of nucleophiles. Cleavage of benzyl linker is achieved

Structure of the Calystegines: New alkaloids of the nortropane family

Three new alkaloids have been isolated from Calystegia sepium; their structures have been established from their 1H and 13C N.M.R. spectra, and confirmed by the synthesis of model compounds.