848075-13-8

Upstream product

• 714293-43-3 (4-trimethylsilylethynyl-2,6-dibromophenyl)(4-tert-butyl-2,6-dimethylphenyl)diazomethane 
• 848075-08-1 ethyl N-nitroso-N-[(2,4,6-tribromophenyl)(4-tert-butyl-2,6-dimethylphenyl)methyl]carbamate 
• 763110-65-2 ethyl N-[(2,4,6-tribromophenyl)(4-tert-butyl-2,6-dimethylphenyl)methyl]carbamate 
• 714293-46-6 (2,4,6-tribromophenyl)(4-tert-butyl-2,6-dimethylphenyl)diazomethane 
• 763110-63-0 (2,4,6-tribromophenyl)(4-tert-butyl-2,6-dimethylphenyl)chloromethane 
• 763110-62-9 (2,4,6-tribromophenyl)(4-tert-butyl-2,6-dimethylphenyl)methanol 
• 45859-98-1 2,4,6-tribromobenzaldehyde 

Downstream Products

• 848075-15-0 2,5-bis{3,5-dibromo-4-(4-tert-butyl-2,6-dimethylphenyldiazomethyl)phenyl}thiophene 

Relevant academic research and scientific papers

Preparation of bis(diazo) compounds incorporated into butadiyne and thiophene units and generation and characterization of their photoproducts

(2,6-Dimethyl-4-tert-butylphenyl)(2,4,6-tribromophenyl)diazomethane(1- N2) was found to be stable enough to survive under Sonogashira coupling reaction conditions, and aryldiazomethyl substituents were introduced at the 1,4-positions of butadiy