102349-15-5

Basic information

• Product Name: (3R,4R)-3-(4-Benzyloxy-3-methoxy-phenyl)-6,7-dimethoxy-2-methyl-1-oxo-1,2,3,4-tetrahydro-isoquinoline-4-carboxylic acid
• CAS NO: 102349-15-5
• Molecular Weight: 477.514
• Mol File: 102349-15-5.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (3R,4R)-3-(4-Benzyloxy-3-methoxy-phenyl)-6,7-dimethoxy-2-methyl-1-oxo-1,2,3,4-tetrahydro-isoquinoline-4-carboxylic acid(CAS DataBase Reference)
• NIST Chemistry Reference: (3R,4R)-3-(4-Benzyloxy-3-methoxy-phenyl)-6,7-dimethoxy-2-methyl-1-oxo-1,2,3,4-tetrahydro-isoquinoline-4-carboxylic acid(102349-15-5)
• EPA Substance Registry System: (3R,4R)-3-(4-Benzyloxy-3-methoxy-phenyl)-6,7-dimethoxy-2-methyl-1-oxo-1,2,3,4-tetrahydro-isoquinoline-4-carboxylic acid(102349-15-5)

Safety Data

• Hazardous Substances Data: 102349-15-5(Hazardous Substances Data)

Upstream product

• 5653-42-9 3,4-dimethoxyhomophthalic anhydride 
• 102349-14-4 [1-(4-Benzyloxy-3-methoxy-phenyl)-meth-(E)-ylidene]-methyl-amine 
• 102349-15-5 (3R,4S)-3-(4-Benzyloxy-3-methoxy-phenyl)-6,7-dimethoxy-2-methyl-1-oxo-1,2,3,4-tetrahydro-isoquinoline-4-carboxylic acid 

Downstream Products

• 102349-15-5 (3R,4R)-3-(4-Benzyloxy-3-methoxy-phenyl)-6,7-dimethoxy-2-methyl-1-oxo-1,2,3,4-tetrahydro-isoquinoline-4-carboxylic acid 
• 102349-18-8 3-(4-Benzyloxy-3-methoxy-phenyl)-6,7-dimethoxy-2-methyl-2H-isoquinolin-1-one 
• 102349-17-7 Acetic acid (3S,4R)-3-(4-benzyloxy-3-methoxy-phenyl)-6,7-dimethoxy-2-methyl-1-oxo-1,2,3,4-tetrahydro-isoquinolin-4-yl ester 
• 102382-23-0 (3S,4R)-3-(4-Hydroxy-3-methoxy-phenyl)-6,7-dimethoxy-2-methyl-1,2,3,4-tetrahydro-isoquinolin-4-ol 
• 102349-19-9 4-(4-Hydroxy-3-methoxy-phenyl)-6,7-dimethoxy-2-methyl-isoquinolinium; chloride 
• 102349-20-2 3-(4-Hydroxy-3-methoxy-phenyl)-6,7-dimethoxy-2-methyl-isoquinolinium; chloride 

Relevant articles and documents

THE SYNTHESIS OF 4-PHENYLISOQUINOLINE FROM A 3-PHENYLISOQUINOLINE BY UTILIZATION OF A NITROGEN ANALOG OF THE PINACOL REARRANGEMENT

The nitrogen analog of the pinacol rearrangement has been utilized for the preparation of a 4-phenylisoquinoline 9 from the intermediate amino alcohol 8.