1042074-04-3

Basic information

• Product Name: 7-(3,4,5-trimethoxyphenyl)-5,6-dihydro-4H-benzo[de]pyrrolo[1,2-a]quinoline
• Synonyms: 7-(3,4,5-trimethoxyphenyl)-5,6-dihydro-4H-benzo[de]pyrrolo[1,2-a]quinoline
• CAS NO: 1042074-04-3
• Molecular Weight: 373.452
• Mol File: 1042074-04-3.mol

Chemical Properties

• CAS DataBase Reference: 7-(3,4,5-trimethoxyphenyl)-5,6-dihydro-4H-benzo[de]pyrrolo[1,2-a]quinoline(CAS DataBase Reference)
• NIST Chemistry Reference: 7-(3,4,5-trimethoxyphenyl)-5,6-dihydro-4H-benzo[de]pyrrolo[1,2-a]quinoline(1042074-04-3)
• EPA Substance Registry System: 7-(3,4,5-trimethoxyphenyl)-5,6-dihydro-4H-benzo[de]pyrrolo[1,2-a]quinoline(1042074-04-3)

Safety Data

• Hazardous Substances Data: 1042074-04-3(Hazardous Substances Data)

Upstream product

• 1042073-75-5 5-(5-bromopent-1-ynyl)-1,2,3-trimethoxybenzene 
• 157017-41-9 1-(2-iodo-phenyl)-1H-pyrrole 

Relevant articles and documents

The versatile role of norbornene in C-H functionalization processes: concise synthesis of tetracyclic fused pyrroles via a threefold domino reaction

The synthesis of novel tetracyclic fused pyrroles from 1-(2-iodophenyl)-1H-pyrrole and various bromoalkyl-aryl alkynes via a palladium(0)-catalyzed and norbornene-mediated threefold domino reaction is reported. PdCl2 and tri-2-furylphosphine (TFP) in the presence of norbornene and Cs2CO3 in CH3CN at 90 °C gave a variety of tetracyclic fused pyrroles in usually high yields. In the described reaction sequence two of the three carbon-carbon bonds are formed by functionalization of an unactivated aryl C-H bond.