320342-75-4

Basic information

• Product Name: methyl 2-(4-(tert-butyl)phenyl)-3-phenylpropanoate
• Synonyms: methyl 2-(4-(tert-butyl)phenyl)-3-phenylpropanoate
• CAS NO: 320342-75-4
• Molecular Weight: 296.409
• Mol File: 320342-75-4.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: methyl 2-(4-(tert-butyl)phenyl)-3-phenylpropanoate(CAS DataBase Reference)
• NIST Chemistry Reference: methyl 2-(4-(tert-butyl)phenyl)-3-phenylpropanoate(320342-75-4)
• EPA Substance Registry System: methyl 2-(4-(tert-butyl)phenyl)-3-phenylpropanoate(320342-75-4)

Safety Data

• Hazardous Substances Data: 320342-75-4(Hazardous Substances Data)

Upstream product

• 3549-23-3 methyl 2-(4-tert-butylphenyl)acetate 
• 100-39-0 benzyl bromide 
• 260783-80-0 N,N,N--trimethyl--1--phenylmethanaminium trifluoromethanesulfonate 

Downstream Products

• 320342-96-9 2-(4-(tert-butyl)phenyl)-3-phenylpropanamide 
• 320343-10-0 2-(4-tert-butyl-phenyl)-3-phenyl-propylamine 
• 320342-83-4 2-(4-tert-butyl-phenyl)-3-phenyl-propionic acid 

Relevant articles and documents

Transition-metal-free and base promoted C-C bond formationviaC-N bond cleavage of organoammonium salts

A transition-metal-free and base promoted C-C bond forming reaction of benzyl C(sp3)-H bond with organoammonium saltsviaC-N bond cleavage has been reported. Benzyl ammonium salts as well as cinnamyl ammonium salt could couple readily with various benzyl C(sp3)-H species, producing the corresponding products in moderate to excellent yields with good functional group tolerance. Late stage chemical manipulation enabled the specific 1,2-diarylethane structure of products transformed into useful olefin compoundsviadehydrogenation, which further demonstrated the utility of this reaction.