196599-46-9

Upstream product

• 540-37-4 p-aminoiodobenzene 
• 159085-28-6 1-(4-iodophenyl)-2-(pyrrolidin-1-yl)diazene 
• 106-40-1 4-bromo-aniline 
• 147227-33-6 1-(4-bromophenyl)-2-(pyrrolidin-1-yl)diazene 
• 196599-76-5 1-(4-trimethylsilylethynylphenyl)-3,3-tetramethylenetriazene 

Downstream Products

• 1404169-63-6 1-[2-(4-ethynylphenyl)diazenyl]pyrrolidine 
• 666839-49-2 4-[3,5-bis(acetylsulfanylmethyl)phenylethynyl]iodobenzene 
• 643764-62-9 3-methoxy-13-methyl-17-[4-(pyrrolidin-1-ylazo)-phenylethynyl]-12,13,14,15,16,17-hexahydro-11H-cyclopenta[a]phenanthren-17-ol 
• 643764-64-1 (8R,9S,13S,14S,17S)-3-Methoxy-13-methyl-17-[4-(pyrrolidin-1-ylazo)-phenylethynyl]-9,11,12,13,14,15,16,17-octahydro-8H-cyclopenta[a]phenanthren-17-ol 
• 643764-59-4 3-O-methyl-17α-{4-[(pyrrolidin-1-yl)-azo]phenylethynyl}estra-1,3,5(10)-trien-3,17β-diol 
• 196599-51-6 5-[4-(Pyrrolidin-1-ylazo)-phenyl]-penta-2,4-diyn-1-ol 

Relevant academic research and scientific papers

Synthesis of triazene-substituted homoconjugated push-pull chromophores by formal [2?+?2] cycloadditions

1-(4-Ethynylphenyl)-3,3-dialkyltriaz-1-enes, well-known building blocks for branched dendrimer syntheses, were utilized as a new type of electron-donor component in formal [2 + 2] cycloadditions. The click-type, atom-economic reactions proceed efficiently

Synthesis of Well-Defined Tower-Shaped 1,3,5-Trisubstituted Adamantanes Incorporating a Macrocyclic Trilactam Ring System

We describe the synthesis of two novel well-defined tower-shaped 1,3,5-trisubstituted adamantanes 30 and 33 that incorporate a macrocyclic trilactam ring system. Each nanoscale molecule has a broad tripodal base consisting of three identical sulfur-contai

Synthesis and radiosynthesis of 17α -[p-(iodophenylethynyl)]estra-3,17β-diols

Estrones have been subjected to an addition reaction with [(4-ethynylphenyl)azo]pyrrolidine to provide 17 α -{4-[(pyrrolidin-1-yl)-azo]phenylethynyl}estra-3,17 β-diols. A subsequent iodination with iodotrimethylsilane, produced in situ from chlorotrimethy