470448-69-2

Basic information

• Product Name: Methanone, [3,4-bis(4-methoxyphenyl)-1H-pyrrole-2,5-diyl]bis[(4-methoxyphenyl)-
• CAS NO: 470448-69-2
• Molecular Formula: C34H29NO6
• Molecular Weight: 547.607
• Mol File: 470448-69-2.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: Methanone, [3,4-bis(4-methoxyphenyl)-1H-pyrrole-2,5-diyl]bis[(4-methoxyphenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Methanone, [3,4-bis(4-methoxyphenyl)-1H-pyrrole-2,5-diyl]bis[(4-methoxyphenyl)-(470448-69-2)
• EPA Substance Registry System: Methanone, [3,4-bis(4-methoxyphenyl)-1H-pyrrole-2,5-diyl]bis[(4-methoxyphenyl)-(470448-69-2)

Safety Data

• Hazardous Substances Data: 470448-69-2(Hazardous Substances Data)

Upstream product

• 100-66-3 methoxybenzene 
• 1027899-57-5 3,4-bis-(4-methoxy-phenyl)-1H-pyrrole-2,5-dicarbonyl dichloride 
• 2234-38-0 3,4-bis(4-methoxyphenyl)-1H-pyrrole-2,5-dicarboxylic acid 
• 100-09-4 4-methoxybenzoic acid 
• 127572-56-9 ethyl 4-(4-methoxyphenyl)-1H-pyrrole-2-carboxylate 
• 848757-55-1 3,4-bis(4-methoxyphenyl)-2-carbethoxy-5-(4-methoxybenzoyl)pyrrole 
• 848757-56-2 3,4-bis(4-methoxyphenyl)-5-(4-methoxybenzoyl)-2-pyrrolecarboxylic acid 
• 848757-48-2 2-(4-methoxybenzoyl)-4-(4-methoxyphenyl)pyrrole 
• 848757-50-6 2,5-bis(4-methoxybenzoyl)-3-iodo-4-(4-methoxyphenyl)pyrrole 
• 5720-07-0 4-methoxyphenylboronic acid 
• 848757-49-3 2,5-bis(4-methoxybenzoyl)-3-(4-methoxyphenyl)pyrrole 
• 848757-53-9 3-iodo-5-(4-methoxybenzoyl)-4-(4-methoxyphenyl)pyrrole-2-carboxylic acid ethyl ester 
• 848757-59-5 3-bromo-2-carbethoxy-5-(4-methoxybenzoyl)-4-(4-methoxyphenyl)pyrrole 

Downstream Products

• 470448-72-7 2,5-bis(4-acetoxy-3,5-dibromobenzoyl)-3,4-bis(4-acetoxy-3,5-dibromophenyl)-1-[2-(4-acetoxyphenyl)ethyl]-1H-pyrrole 
• 470448-71-6 2,5-bis(4-acetoxy-3,5-dibromobenzoyl)-3,4-bis(4-acetoxy-3,5-dibromophenyl)-1H-pyrrole 
• 272118-06-6 polycitone B 
• 153212-84-1 Polycitone A 
• 470448-70-5 2,5-bis(4-hydroxybenzoyl)-3,4-bis(4-hydroxyphenyl)-1H-pyrrole 

Relevant articles and documents

The application of vinylogous iminium salt derivatives to an efficient relay synthesis of the pyrrole containing alkaloids polycitone A and B

A new and efficient relay synthesis of the marine natural products polycitone A and B is described. The new strategy relies on the formation of 2,4-disubstituted pyrroles from a vinamidinium salt followed by electrophilic substitution at the 5-position of