4303-71-3

Basic information

• Product Name: TRIPHENYLMETHYL SODIUM
• Synonyms: TRIPHENYLMETHYL SODIUM;triphenylmethylsodium25%ineptane
• CAS NO: 4303-71-3
• Molecular Formula: C₁₉H₁₅*Na
• Molecular Weight: 266.31
• Mol File: 4303-71-3.mol
• Article Data: 2

Chemical Properties

• Appearance: /
• CAS DataBase Reference: TRIPHENYLMETHYL SODIUM(CAS DataBase Reference)
• NIST Chemistry Reference: TRIPHENYLMETHYL SODIUM(4303-71-3)
• EPA Substance Registry System: TRIPHENYLMETHYL SODIUM(4303-71-3)

Safety Data

• Hazardous Substances Data: 4303-71-3(Hazardous Substances Data)

Upstream product

• 519-73-3 triphenylmethane 
• 1623-99-0 phenyl sodium 
• 76-83-5 trityl chloride 
• 2216-49-1 triphenylmethyl radical 
• 60-29-7 diethyl ether 
• 854218-28-3 2-biphenyl-4-yl-1,1,1,2-tetraphenyl-ethane 
• 71-43-2 benzene 
• 41050-17-3 2,2-bis-(4-methoxy-phenyl)-1,1,1-triphenyl-ethane 
• 19112-42-6 pentaphenylethane 
• 7664-41-7 ammonia 
• 109-99-9 tetrahydrofuran 
• 112715-27-2 α-phenoxy-benzhydryl sodium 

Downstream Products

• 2294-95-3 5,5,5-Triphenyl-1-pentanol 
• 896-32-2 2,2,2-triphenylethanol 
• 630-76-2 tetraphenylmethane 
• 1902-03-0 2-isopropyl-5-methyl-3-oxo-hexanoic acid ethyl ester 
• 116773-05-8 ethyl 2-benzoyl-2-ethylbutanoate 
• 16928-73-7 triphenylmethyl phenyl sulfide 
• 87655-70-7 pentaphenyl-ethyl 
• 16636-62-7 1-(2'-hydroxyphenyl)butane-1,3-dione 
• 4895-47-0 tetraphenoxyethene 
• 861096-03-9 1-(4-benzhydryl-phenyl)-2,2,2-triphenyl-ethanone 
• 451-40-1 phenyl benzyl ketone 
• 519-73-3 triphenylmethane 
• 596-30-5 ditrityl peroxide 
• 108-95-2 phenol 

Relevant articles and documents

Preparation and Characterization of Some Pentaarylethyls

The reaction of triphenylmethylsodium with dichlorodiphenylmethane does not give pentaphenylethyl as previously reported, but when the anion reacts with 9,9-dichlorofluorene, it does form the reported 9-tritylfluorenyl radical which has been characterized by ESR spectroscopy.The radical is better prepared by oxidation of the anion of 9-tritylfluorene.The 9-tritylfluorenyl radical reacts with traces of oxygen to give triphenylmethyl and fluorenone.With light it forms triphenylmethyl and fluorenylidene.The latter was established by photolyzing 9-diazofluorene in the presence of triphenylmethyl with the generation of 9-tritylfluorenyl.Small yields of the persistent pentakis(p-tert-butylphenyl)ethyl radical have been prepared, and it is propable that pentaphenylethyl has also.