1260507-07-0

Basic information

• Product Name: phenyl-(1-(2,4,6-trimethoxyphenyl)-3,4-dihydroisoquinolin-2(1H)-yl)methanone
• Synonyms: phenyl-(1-(2,4,6-trimethoxyphenyl)-3,4-dihydroisoquinolin-2(1H)-yl)methanone
• CAS NO: 1260507-07-0
• Molecular Weight: 403.478
• Mol File: 1260507-07-0.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: phenyl-(1-(2,4,6-trimethoxyphenyl)-3,4-dihydroisoquinolin-2(1H)-yl)methanone(CAS DataBase Reference)
• NIST Chemistry Reference: phenyl-(1-(2,4,6-trimethoxyphenyl)-3,4-dihydroisoquinolin-2(1H)-yl)methanone(1260507-07-0)
• EPA Substance Registry System: phenyl-(1-(2,4,6-trimethoxyphenyl)-3,4-dihydroisoquinolin-2(1H)-yl)methanone(1260507-07-0)

Safety Data

• Hazardous Substances Data: 1260507-07-0(Hazardous Substances Data)

Upstream product

• 82342-56-1 N-benzoyl-1,2,3,4-tetrahydroisoquinoline 
• 621-23-8 1,2,3-trimethoxybenzene 

Relevant articles and documents

Bronsted acid catalyzed C-H functionalization of N-protected tetrahydroisoquinolines via intermediate peroxides

An organocatalytic oxidative synthesis of N-protected tetrahydroisoquinolines is described by C-H functionalization via intermediate peroxides. The peroxides were synthesized from tert-butylhydroperoxide under metal-free thermal conditions and were converted into the final products by Bronsted acid catalyzed substitution. The nucleophile scope was investigated in detail and proved to be broad; N-deprotection of the coupling products could also be achieved. An organocatalytic oxidative synthesis of N-protected tetrahydroisoquinolines was achieved by C-H functionalization via Intermediate PeroxideS (CHIPS). The peroxides were synthesized under metal-free thermal conditions and were converted into the final products by reaction with a variety of nucleophiles by using Bronsted acid catalysis. Copyright

Facile, solvent and ligand free iron catalyzed direct functionalization of N-protected tetrahydroisoquinolines and isochroman

An efficient method for an iron catalyzed oxidative indolation and methoxyphenylation of N-protected tetrahydroisoquinolines and isochroman is described including subsequent facile deprotection. The Royal Society of Chemistry 2010.