106674-00-4

Basic information

• Product Name: (E)-benzyl 3-<1-((4-methylphenyl)sulphonyl)-5-(methoxycarbonyl)-pyrrol-3-yl>acrylate
• Synonyms: (E)-benzyl 3-<1-((4-methylphenyl)sulphonyl)-5-(methoxycarbonyl)-pyrrol-3-yl>acrylate
• CAS NO: 106674-00-4
• Molecular Weight: 439.489
• Mol File: 106674-00-4.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: (E)-benzyl 3-<1-((4-methylphenyl)sulphonyl)-5-(methoxycarbonyl)-pyrrol-3-yl>acrylate(CAS DataBase Reference)
• NIST Chemistry Reference: (E)-benzyl 3-<1-((4-methylphenyl)sulphonyl)-5-(methoxycarbonyl)-pyrrol-3-yl>acrylate(106674-00-4)
• EPA Substance Registry System: (E)-benzyl 3-<1-((4-methylphenyl)sulphonyl)-5-(methoxycarbonyl)-pyrrol-3-yl>acrylate(106674-00-4)

Safety Data

• Hazardous Substances Data: 106674-00-4(Hazardous Substances Data)

Upstream product

• 98-59-9 p-toluenesulfonyl chloride 
• 40611-79-8 methyl 4-formyl-1H-pyrrole-2-carboxylate 
• 7396-44-3 benzyl diethylphosphonoacetate 
• 106673-99-8 4-Formyl-1-(toluene-4-sulfonyl)-1H-pyrrole-2-carboxylic acid methyl ester 
• 1193-62-0 methyl Pyrrole-2-carboxylate 

Downstream Products

• 106674-04-8 C₃₃H₃₅N₂O₁₁PS 
• 106674-05-9 benzyl 3,6-dihydro-4-((diethoxyphosphinyl)oxy)-5-hydroxy-7-(methyloxycarbonyl)-6-((4-methylphenyl)sulfonyl)benzo<1,2-b:4,3-b'>dipyrrole-1-carboxylate 
• 106674-02-6 2-Chlorooxalyl-1'-(toluene-4-sulfonyl)-1H,1'H-[3,3']bipyrrolyl-4,5'-dicarboxylic acid 4-benzyl ester 5'-methyl ester 
• 106674-03-7 benzyl 7-(methoxycarbonyl)-3,4,5,6-tetrahydro-4,5-dioxo-6-((4-methylphenyl)sulfonyl)benzo<1,2-b:4,3-b'>dipyrrole-1-carboxylate 
• 106674-01-5 benzyl 5-(methoxycarbonyl)-1-((4-methylphenyl)sulfonyl)-3,3'-bipyrrole-4'-carboxylate 

Relevant articles and documents

Studies on the Synthesis of the Antitumor Agent CC-1065. Synthesis of PDE I and PDE II, Inhibitors of Cyclic Adenosine-3',5'-monophosphate Phosphodiesterase Using the 3,3'-Bipyrrole Strategy

In the model series tert-butyl 2,4-pentadienoate was treated with TosCHMeNC/NaH to give the pyrrole 18, which was converted into the 3,3'-bipyrrole 20.Treatment of the pyrrole 20 with oxalyl chloride gave the o-quinone 21, which was reduced and concomitan