714293-43-3

Upstream product

• 1066-54-2 trimethylsilylacetylene 
• 714293-46-6 (2,4,6-tribromophenyl)(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 
• 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 
• 5345-05-1 4-t-butyl-2,6-dimethylbromobenzene 

Downstream Products

• 714293-44-4 [2,4-bis(trimethylsilylethynyl)-6-bromophenyl](4-tert-butyl-2,6-dimethylphenyl)diazomethane 
• 848075-15-0 2,5-bis{3,5-dibromo-4-(4-tert-butyl-2,6-dimethylphenyldiazomethyl)phenyl}thiophene 
• 848075-13-8 1,4-bis{3,5-dibromo-4-(4-tert-butyl-2,6-dimethylphenyldiazomethyl)phenyl}butadiyne 
• 714293-45-5 [2,4,6-tris(trimethylsilylethynyl)phenyl](4-tert-butyl-2,6-dimethylphenyl)diazomethane 
• 714293-50-2 C₃₄H₄₆Si₃ 
• 714293-49-9 C₂₉H₃₇BrSi₂ 
• 763110-74-3 (3,5-bis-{3,5-dibromo-4-[(4-tert-butyl-2,6-dimethyl-phenyl)-diazo-methyl]-phenylethynyl}-phenylethynyl)-trimethyl-silane 
• 763110-67-4 (2,6-dibromo-4-ethynylphenyl)-(2,6-dimethyl-4-tert-butylphenyl)diazomethane 
• 714293-48-8 (4-trimethylsilyl-2,6-dibromophenyl)(4-tert-butyl-2,6-dimethylphenyl)carbene 

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

Preparation of poly(phenyl)acetylenes having diazo groups and magnetic characterization of poly(carbene)

(2,6-Dibromo-4-ethynylphenyl)(2,6-dimethyl-4-tert-butylphenyl)diazomethane was found to be stable enough to survive under Rh-complex-catalyzed polymerization conditions and underwent polymerization to give a phenylacetylene polymer having diazo functional

Synthesis of phenylacetylene dendrimers having sterically congested diazo units and characterization of their photoproducts

The compound (4-tert-butyl-2,6-dimethylphenyl)(2,4,6-tribromophenyl) diazomethane (1a), a precursor for persistent triplet carbene, was found to be stable enough to survive Sonogashira coupling reaction conditions to give (4-tertbutyl-2,6-dimethylphenyl)(

Triplet diphenylcarbenes protected by (trimethylsilyl)ethynyl groups

(2,4,6-Tribromophenyl)(4-tert-butyl-2,6-dimethylphenyl)diazomethane (1a) was shown to be stable enough to survive Sonogashira coupling reaction conditions at an elevated temperature and gave not only a para-monosubstituted product, (4-trimethylsilylethyny