914607-22-0

Basic information

• Product Name: methyl 5-(2,5-dimethoxybenzyl)-7-methoxy-2-methyl-1-oxo-2,3-dihydro-1H-isoindole-4-carboxylate
• Synonyms: methyl 5-(2,5-dimethoxybenzyl)-7-methoxy-2-methyl-1-oxo-2,3-dihydro-1H-isoindole-4-carboxylate
• CAS NO: 914607-22-0
• Molecular Weight: 385.417
• Mol File: 914607-22-0.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: methyl 5-(2,5-dimethoxybenzyl)-7-methoxy-2-methyl-1-oxo-2,3-dihydro-1H-isoindole-4-carboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: methyl 5-(2,5-dimethoxybenzyl)-7-methoxy-2-methyl-1-oxo-2,3-dihydro-1H-isoindole-4-carboxylate(914607-22-0)
• EPA Substance Registry System: methyl 5-(2,5-dimethoxybenzyl)-7-methoxy-2-methyl-1-oxo-2,3-dihydro-1H-isoindole-4-carboxylate(914607-22-0)

Safety Data

• Hazardous Substances Data: 914607-22-0(Hazardous Substances Data)

Upstream product

• 914607-14-0 methyl 7-methoxy-2-methyl-1-oxo-5-(trifluoromethanesulfonyloxy)-2,3-dihydro-1H-isoindole-4-carboxylate 
• 352530-32-6 2,5-dimethoxy-benzylzinc chloride 
• 914607-17-3 methyl 5,7-dimethoxy-2-methyl-1-oxo-2,3-dihydro-1H-isoindole-4-carboxylate 
• 914607-16-2 methyl 5,7-dimethoxy-1-oxo-2,3-dihydro-1H-isoindole-4-carboxylate 
• 914607-33-3 5-hydroxy-7-methoxy-2-methyl-1-oxo-2,3-dihydro-1H-isoindole-4-carboxylic acid methyl ester 
• 914607-15-1 dimethyl 2-cyano-4,6-dimethoxy-1,3-benzenedicarboxylate 
• 914607-32-2 4,6-dimethoxy-2-trifluoromethanesulfonyloxy-isophthalic acid dimethyl ester 
• 51116-92-8 methyl 4,6-dimethoxysalicylate 
• 51116-93-9 3-Formyl-2-hydroxy-4,6-dimethoxy-benzoesaeuremethylester 
• 29723-28-2 methyl 2,4,6-trimethoxybenzoate 
• 773875-93-7 dimethyl 2-hydroxy-4,6-dimethoxy-1,3-benzenedicarboxylate 

Downstream Products

• 914607-23-1 5-(2,5-dimethoxybenzyl)-7-methoxy-2-methyl-1-oxo-2,3-dihydro-1H-isoindole-4-carboxylic acid 

Relevant articles and documents

Studies on the total synthesis of lactonamycin: Synthesis of the CDEF ring system

A concise and efficient synthesis of the tetracyclic CDEF ring system of lactonamycin (1) is described. The key step involved the Lewis acid mediated, intramolecular Friedel-Crafts acylation of carboxylic acid 6 to produce the tetracyclic CDEF core struct