648418-76-2

Upstream product

• 90-44-8 anthracen-9(10H)-one 
• 5345-05-1 4-t-butyl-2,6-dimethylbromobenzene 
• 648418-75-1 9-(4-tert-butyl-2,6-dimethylphenyl)anthracene 

Downstream Products

• 853732-44-2 10-(4-tert-butyl-2,6-dimethylphenyl)anthracene-9-carbaldehyde 
• 648418-80-8 ethyl N-nitroso-N-methyl-bis{9-[10-(4-tert-butyl-2,6-dimethyl)phenyl]anthryl}carbamate 
• 666257-70-1 3,5-bis{3,5-dimethyl-4-(diazo[9-{10-(4-tert-butyl-2,6-dimethylphenyl)anthryl}]methyl)phenyl}benzene 
• 666257-69-8 [9-{10-(4-tert-butyl-2,6-dimethylphenyl)anthryl}](4-phenyl-2,6-dimethylphenyl)diazomethane 
• 853732-45-3 [10-(4-tert-butyl-2,6-dimethylphenyl)-9-anthryl][2,7-dibromo-10-(4-tert-butyl-2,6-dimethylphenyl)-9-anthryl]methanol 
• 875052-19-0 [3-bromo-10-(4-t-butyl-2,6-dimethylphenyl)-9-anthryl][10-(4-t-butyl-2,6-dimethylphenyl)-9-anthryl]methanol 
• 648418-77-3 di{9-[10-(4-tert-butyl-2,6-dimethyl)phenyl]anthryl}methanol 
• 666257-67-6 ethyl N-nitroso-N-[9-{10-(4-tert-butyl-2,6-dimethylphenyl)anthryl}]{(4-bromo-2,6-dimethylphenyl)methyl}carbamate 
• 666257-66-5 ethyl [9-{10-(4-(t-butyl)-2,6-dimethylphenyl)}anthryl](4-bromo-2,6-dimethylphenyl)methylcarbamate 
• 666257-68-7 [9-{10-(4-tert-butyl-2,6-dimethylphenyl)anthryl}](4-bromo-2,6-dimethylphenyl)diazomethane 
• 666257-65-4 [9-{10-(4-tert-butyl-2,6-dimethylphenyl)anthryl}](4-bromo-2,6-dimethylphenyl)chloromethane 
• 768381-82-4 1,4-bis(3,5-dimethyl-4-[9-{10-(4-(t-butyl)-2,6-dimethylphenyl)}anthryl]diazomethylphenyl)butadiyne 
• 768381-83-5 2,5-bis(3,5-dimethyl-4-[9-{10-(4-(t-butyl)-2,6-dimethylphenyl)}anthryl]diazomethylphenyl)thiophene 
• 768381-81-3 [9-{10-(4-(t-butyl)-2,6-dimethylphenyl)}anthryl][2,6-dimethyl-4-(trimethylsilylethynyl)phenyl]diazomethane 

Relevant academic research and scientific papers

A tris(carbene) constructed with stable triplet carbene units

Bis[10-(4-t-butyl-2,6-dimethylphenyl)-9-anthryl]diazomethane, which can generate a fairly stable triplet carbene that can survive for even a week in solution at room temperature, was shown to be stable enough to undergo a Sonogashira coupling reaction. Th

Preparation of Oligodiazo Compounds by Using the Suzuki Coupling Reaction and Characterization of Their Photoproducts

[9-{10-(4-tert-Butyl-2,6-dimethyl)phenyl}anthryl](4-bromo-2, 6-dimethylphenyl)diazomethane was found to be stable enough to survive under Suzuki coupling conditions and underwent mono-, di-, and trisubstitution with benzene mono-, di-, and triboronic acid

Preparation of bis(diazo) compounds incorporated into butadiyne and thiophene units, and generation and characterization of Bis(carbene) from these compounds

[9-{10-(4-t-Butyl-2,6-dimethyl)phenyl}anthryl](4-bromo-2,6-dimethylphenyl) diazomethane(1-N2) was found to be stable enough to survive under Sonogashira and Suzuki coupling reaction conditions, and bis(diazo) compounds incorporated into the 1,4

A Triplet Carbene Surviving a Week in Solution at Room Temperature

A stable triplet carbene, having a lifetime at 25 °C of 14.5 days in a dilute benzene solution, was realized by simply changing the substituent at the 10 position of the previously most persistent carbene, di[9-(10-phenyl)anthryl]carbene, from a phenyl to