1228320-14-6

Basic information

• Product Name: methyl 2-(4-methoxybenzyl)-2-methylpropanoate
• Synonyms: methyl 2-(4-methoxybenzyl)-2-methylpropanoate
• CAS NO: 1228320-14-6
• Molecular Weight: 210.248
• Mol File: 1228320-14-6.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: methyl 2-(4-methoxybenzyl)-2-methylpropanoate(CAS DataBase Reference)
• NIST Chemistry Reference: methyl 2-(4-methoxybenzyl)-2-methylpropanoate(1228320-14-6)
• EPA Substance Registry System: methyl 2-(4-methoxybenzyl)-2-methylpropanoate(1228320-14-6)

Safety Data

• Hazardous Substances Data: 1228320-14-6(Hazardous Substances Data)

Upstream product

• 547-63-7 Methyl isobutyrate 
• 459-46-1 4-Fluorobenzyl bromide 
• 31469-15-5 1-methoxy-2-methyl-1-trimethylsiloxy-1-propene 
• 502-00-1 p-fluorobenzyl acetate 

Downstream Products

• 1429923-88-5 2-(4-fluorobenzyl)-3-(4-methoxyphenyl)-2-methyl-N-(quinolin-8-yl)propanamide 
• 1429896-56-9 3-(4-fluorophenyl)-2,2-dimethyl-N-(quinolin-8-yl)propanamide 
• 676621-96-8 3-(4-Fluorophenyl)-2,2-dimethyl-propionic Acid 
• 1613145-97-3 3-(4-fluorobenzyl)-3-methyl-1-(8-quinolinyl)-2-azetidinone 
• 1613146-04-5 4-(4-fluorophenyl)-3,3-dimethyl-1-(8-quinolinyl)-2-azetidinone 

Relevant articles and documents

Copper-catalyzed intramolecular C(sp3)-H and C(sp2)-H amidation by oxidative cyclization

The first copper-catalyzed intramolecular C(sp3)-H and C(sp 2)-H oxidative amidation has been developed. Using a Cu(OAc) 2 catalyst and an Ag2CO3 oxidant in dichloroethane solvent, C(sp3)-H

Trialkylsilyl triflimides as easily tunable organocatalysts for allylation and benzylation of silyl carbon nucleophiles with non-genotoxic reagents

Trialkylsilyl triflimides generated in situ are unique catalysts for the electrophilic benzylation or allylation of trialkylsilylenol ethers or allyl trialkylsilanes with non-genotoxic alkylating reagents such as benzyl and allyl acetates. In most cases the reactions are fast at room temperature and yields are high. The reaction works particularly well with electron-rich benzyl donors including derivatives of pyrrole, indole and furane.