51747-44-5

Basic information

• Product Name: α-(p-nitrophenyl)acrylic acid
• Synonyms: α-(p-nitrophenyl)acrylic acid
• CAS NO: 51747-44-5
• Molecular Weight: 193.159
• Mol File: 51747-44-5.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: α-(p-nitrophenyl)acrylic acid(CAS DataBase Reference)
• NIST Chemistry Reference: α-(p-nitrophenyl)acrylic acid(51747-44-5)
• EPA Substance Registry System: α-(p-nitrophenyl)acrylic acid(51747-44-5)

Safety Data

• Hazardous Substances Data: 51747-44-5(Hazardous Substances Data)

Upstream product

• 13797-13-2 α-(p-nitrophenyl)-β-(N-piperidyl)propionic aicd 
• 104-03-0 4-nitrobenzeneacetic acid 
• 7732-18-5 water 

Downstream Products

• 103297-89-8 4-aza-4-cyclohexyl-2-(4-nitrophenyl)-1,6-heptadiene-3,5-dione 
• 28042-33-3 1,2-Di(4-nitrophenyl)cyclobuten 
• 28131-18-2 cis-1,2-Dimethoxycarbonyl-1,2-bis(4-nitrophenyl)cyclobutan 
• 103298-13-1 1,5-di-(4-nitrophenyl)-3-n-propyl-3-azabicyclo[3.1.1]heptane-2,4-dione 
• 103298-14-2 2-(4-Nitro-phenyl)-N-[2-(4-nitro-phenyl)-acryloyl]-N-propyl-acrylamide 
• 103297-90-1 3-(4-methoxybenzyl)-1-(4-nitrophenyl)-3-azabicyclo[3.1.1]heptane-2,4-dione 
• 103297-81-0 3-n-decyl-1-(4-nitrophenyl)-3-azabicyclo[3.1.1]-heptane-2,4-dione 
• 103297-84-3 3-cyclohexylmethyl-1-(4-nitrophenyl)-3-azabicyclo-[3.1.1]heptane-2,4-dione 
• 103297-82-1 4-aza-4-n-decyl-2-(4-nitrophenyl)-1,6-heptadiene-3,5-dione 
• 103298-12-0 1,5-di-(4-aminophenyl)-3-n-propyl-3-azabicyclo[3.1.1]heptane-2,4-dione 
• 103297-88-7 3-cyclohexyl-1-(4-nitrophenyl)-3-azabicyclo[3.1.1]-heptane-2,4-dione 
• 103298-33-5 3-n-heptyl-1-(4-nitrophenyl)-3-azabicyclo[3.1.1]heptane-2,4-dione 
• 103297-95-6 3-benzyl-1-(4-nitrophenyl)-3-azabicyclo[3.1.1]heptane-2,4-dione 
• 103312-56-7 1-(4-aminophenyl)-3-(4-methoxybenzyl)-3-azabicyclo[3.1.1]heptane-2,4-dione 

Relevant articles and documents

Intramolecular Carbenoid Reactions of Pyrrole Derivatives. A Total Synthesis of (+/-)-Ipalbidine

A mew method for alkaloid synthesis is described.The rhodium(II)-acetate-catalyzed decomposition of 3-(4-acetoxyphenyl)-1-diazo-4-(pyrrol-1-yl)-2-butanone (5d) gave 6-(4-acetoxyphenyl)-5,6-dihydro-7(8H)-indolizinone (6d) in 82percent yield via an intramolecular carbenoid reaction.The latter compound was converted in four steps in 13percent overall yield to (+/-)-ipalbidine (1b).