951771-24-7

Basic information

• Product Name: bis(2-methoxy-5-methylphenyl)phenylmethane
• Synonyms: bis(2-methoxy-5-methylphenyl)phenylmethane
• CAS NO: 951771-24-7
• Molecular Weight: 332.442
• Mol File: 951771-24-7.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: bis(2-methoxy-5-methylphenyl)phenylmethane(CAS DataBase Reference)
• NIST Chemistry Reference: bis(2-methoxy-5-methylphenyl)phenylmethane(951771-24-7)
• EPA Substance Registry System: bis(2-methoxy-5-methylphenyl)phenylmethane(951771-24-7)

Safety Data

• Hazardous Substances Data: 951771-24-7(Hazardous Substances Data)

Upstream product

• 36359-93-0 2,2′-(phenylmethylene)bis(4-methylphenol) 
• 104-93-8 p-methylanizole 
• 100-52-7 benzaldehyde 
• 51608-60-7 phenyl N-tosyl imine 

Relevant articles and documents

Room-temperature bismuth-catalyzed bis-arylation of carbonyl compounds with aryl ethers and phenols

Using Bi2(SO4)3 as the catalyst and TMSCl as the additive, a wide variety of aldehydes, ketones, and acetals were smoothly condensed with aryl ethers at room temperature to provide the corresponding diarylmethanes and triarylmethanes selectively in good to excellent yields. Using Bi2(SO4)3 as the catalyst and TMSCl as the additive, a wide variety of aldehydes, ketones, and acetals were smoothly condensed with aryl ethers at room temperature to selectively provide the corresponding diarylmethanes and triarylmethanes in good to excellent yields. Copyright

Catalytic selective bis-arylation of imines with anisole, phenol, thioanisole and analogues

The first highly efficient double Friedel-Crafts reaction of N-tosyl imines with anisole, phenol, thioanisole and analogues has been developed to produce the corresponding symmetric diarylmethanes and triarylmethanes with high regioselectivity in the presence of a catalytic amount of Bi2(SO 4)3-TMSCl at room temperature. The Royal Society of Chemistry.