882866-44-6

Basic information

• Product Name: 3-iodo-2-(4'-methoxyphenyl)-quinolin-4(1H)-one
• Synonyms: 3-iodo-2-(4'-methoxyphenyl)-quinolin-4(1H)-one
• CAS NO: 882866-44-6
• Molecular Weight: 377.181
• Mol File: 882866-44-6.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 3-iodo-2-(4'-methoxyphenyl)-quinolin-4(1H)-one(CAS DataBase Reference)
• NIST Chemistry Reference: 3-iodo-2-(4'-methoxyphenyl)-quinolin-4(1H)-one(882866-44-6)
• EPA Substance Registry System: 3-iodo-2-(4'-methoxyphenyl)-quinolin-4(1H)-one(882866-44-6)

Safety Data

• Hazardous Substances Data: 882866-44-6(Hazardous Substances Data)

Upstream product

• 1027223-95-5 methyl (Z)-N-{2-[(trimethylsilyl)ethynyl]phenyl}benzimidate 
• 1433174-92-5 N-methoxy-3-(4-methoxyphenyl)-N-methylpropiolamide 
• 615-43-0 2-iodophenylamine 
• 33768-41-1 N-(2-acetyl-phenyl)-4-methoxy-benzamide 
• 100-07-2 4-methoxy-benzoyl chloride 
• 551-93-9 2-aminoacetophenone 
• 1433175-08-6 C₂₄H₁₉NO₃ 
• 768-60-5 4-methoxyphenylacetylen 
• 3813-92-1 2-(4-methoxyphenyl)-1,4-dihydro-4-oxoquinoline 

Downstream Products

• 1309362-54-6 N-(2-(4-methoxyphenyl)-1-methyl-4-oxo-1,4-dihydroquinolin-3-yl)acetamide 
• 1309362-45-5 4-methoxy-N-(2-(4-methoxyphenyl)-1-methyl-4-oxo-1,4-dihydroquinolin-3-yl)benzamide 
• 246181-55-5 1-methyl-2-(4’-methoxyphenyl)-1H-4-quinolone 
• 1079284-15-3 4-chloro-3-iodo-2-(4'-methoxyphenyl)quinoline 
• 876460-09-2 3-iodo-2-(4'-methoxyphenyl)-1-methylquinolin-4(1H)-one 

Relevant articles and documents

Photoredox halogenation of quinolones: The dual role of halo-fluorescein dyes

An efficient C-3 halogenation of quinolin-4-ones is reported with halogenated fluorescein dyes which serve both as a halogen source and photocatalyst. This reaction shows broad substrate scope and gives good to excellent yields of C-3 brominated/iodinated

Scaffold-divergent synthesis of ring-fused indoles, quinolines, and quinolones via iodonium-induced reaction cascades

N-(2-Iodophenyl)imines A are readily formed from Schiff's base condensation of 2-iodoanilines with carbonyls and ketals. These imines provide useful substrates in scaffold-divergent synthesis through the attachment of an alkyne (Songashira coupling or acyl substitution of a Weinreb amide) followed by an iodonium-induced reaction cascade to give ring-fused indoles B, quinolines C, or quinolones D depending on the reaction conditions employed.