1428338-98-0

Basic information

• Product Name: 1-((4-(tert-butyl)phenyl)(3-methoxyphenyl)methyl)-3-methylbenzene
• Synonyms: 1-((4-(tert-butyl)phenyl)(3-methoxyphenyl)methyl)-3-methylbenzene
• CAS NO: 1428338-98-0
• Molecular Weight: 344.497
• Mol File: 1428338-98-0.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 1-((4-(tert-butyl)phenyl)(3-methoxyphenyl)methyl)-3-methylbenzene(CAS DataBase Reference)
• NIST Chemistry Reference: 1-((4-(tert-butyl)phenyl)(3-methoxyphenyl)methyl)-3-methylbenzene(1428338-98-0)
• EPA Substance Registry System: 1-((4-(tert-butyl)phenyl)(3-methoxyphenyl)methyl)-3-methylbenzene(1428338-98-0)

Safety Data

• Hazardous Substances Data: 1428338-98-0(Hazardous Substances Data)

Upstream product

• 71372-40-2 (3-methoxyphenyl)(m-tolyl)methanone 
• 3972-65-4 1-bromo-4-tert-butylbenzene 
• 1428362-12-2 C₂₂H₂₂N₂O₃S 

Relevant articles and documents

Synthesis of Di- and Triarylmethanes through Palladium-Catalyzed Reductive Coupling of N -Tosylhydrazones and Aryl Bromides

A palladium-catalyzed reductive coupling between N-tosylhydrazones and aryl bromides has been developed. The reaction provides an efficient method for the synthesis of diarylmethanes and triarylmethanes via the formation of C(sp2)-C(sp3) single bonds. This new methodology for the synthesis of diarylmethanes and triarylmethanes is featured by the ready availability of the starting materials, mild reaction conditions, and the tolerance of wide range of functional groups. The reaction follows a pathway including palladium carbene formation, migratory insertion, and reduction of the alkylpalladium(II) intermediate.