1245527-80-3

Basic information

• Product Name: 1-(3,4-dimethoxybenzyl)-4-methoxy-2-(methoxycarbonyl)pyridinium bromide salt
• Synonyms: 1-(3,4-dimethoxybenzyl)-4-methoxy-2-(methoxycarbonyl)pyridinium bromide salt
• CAS NO: 1245527-80-3
• Molecular Weight: 398.254
• Mol File: 1245527-80-3.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 1-(3,4-dimethoxybenzyl)-4-methoxy-2-(methoxycarbonyl)pyridinium bromide salt(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(3,4-dimethoxybenzyl)-4-methoxy-2-(methoxycarbonyl)pyridinium bromide salt(1245527-80-3)
• EPA Substance Registry System: 1-(3,4-dimethoxybenzyl)-4-methoxy-2-(methoxycarbonyl)pyridinium bromide salt(1245527-80-3)

Safety Data

• Hazardous Substances Data: 1245527-80-3(Hazardous Substances Data)

Upstream product

• 21852-32-4 4-bromomethyl-1,2-dimethoxybenzene 
• 29681-43-4 methyl 4-methoxypicolinate 

Downstream Products

• 1245527-84-7 methyl-1-(3,4-dimethoxybenzyl)-2-methyl-4-oxo-1,2,3,4-tetrahydropyridine-2-carboxylate 
• 1245527-85-8 methyl-1-(3,4-dimethoxybenzyl)-2-ethyl-4-oxo-1,2,3,4-tetrahydropyridine-2-carboxylate 
• 1245527-98-3 methyl-1-(3,4-dimethoxybenzyl)-4-oxo-6-(prop-1-ynyl)-1,4,5,6-tetrahydropyridine-2-carboxylate 
• 1245527-87-0 methyl-1-(3,4-dimethoxybenzyl)-4-oxo-6-vinyl-1,4,5,6-tetrahydropyridine-2-carboxylate 
• 1245527-95-0 methyl-1-(3,4-dimethoxybenzyl)-4-oxo-6-(prop-1-en-2-yl)-1,4,5,6-tetrahydropyridine-2-carboxylate 
• 1245527-90-5 methyl-2-(but-3-enyl)-1-(3,4-dimethoxybenzyl)-4-oxo-1,2,3,4-tetrahydropyridine-2-carboxylate 
• 1245527-96-1 methyl-2-benzyl-1-(3,4-dimethoxybenzyl)-4-oxo-1,2,3,4-tetrahydropyridine-2-carboxylate 
• 1245528-00-0 methyl-2-(4-chlorobutyl)-1-(3,4-dimethoxybenzyl)-4-oxo-1,2,3,4-tetrahydropyridine-2-carboxylate 
• 1245527-82-5 methyl-1-(3,4-dimethoxybenzyl)-4-oxo-6-phenyl-1,4,5,6-tetrahydropyridine-2-carboxylate 
• 1245527-93-8 methyl-1-(3,4-dimethoxybenzyl)-6-(4-methoxyphenyl)-4-oxo-1,4,5,6-tetrahydropyridine-2-carboxylate 

Relevant articles and documents

Synthesis of cylindricine C and a formal synthesis of cylindricine A

This paper reports the synthesis of the alkaloid natural product (±)-cylindricine C, in addition to a formal synthesis of (±)-cylindricine A. The key step in our sequence is the (ipso) regioselective addition of an alkyl Grignard reagent to a C-2 substitu