129541-86-2

Upstream product

• 136881-85-1 6-[3-(tert-Butyl-hydroxy-amino)-4-chloro-phenyl]-2-methyl-hexa-3,5-diyn-2-ol 
• 106-39-8 bromochlorobenzene 
• 873-73-4 4-n-chlorophenylacetylene 
• 136881-87-3 1-(p-chlorophenyl)-5-methyl-1,3-hexadiyn-5-ol 
• 136881-88-4 1-(p-chlorophenyl)-5-methyl-1,3-hexadiyn-5-ol tetrahydropyranyl ether 
• 136881-89-5 1-<3-(N-tert-butylhydroxyamino)-4-chlorophenyl>-5-methyl-1,3-hexadiyn-5-ol tetrahydropyranyl ether 

Downstream Products

• 147986-92-3 8-[3-(tert-Butyl-hydroxy-amino)-4-chloro-phenyl]-2-methyl-octa-3,5,7-triyn-2-ol 
• 147986-93-4 N-tert-Butyl-N-(2-chloro-5-hexa-1,3,5-triynyl-phenyl)-hydroxylamine 
• 129541-88-4 1-<4-Chloro-3-(N-tert-butyl-N-oxylamino)phenyl>-1,3-butadiyne 

Relevant academic research and scientific papers

An approach to organic ferromagnets. Synthesis and characterization of 1-phenyl-1,3-butadiyne polymers having a persistent nitroxide group on the phenyl ring

1-[3-(N-tert-Butylhydroxyamino)-4-chlorophenyl]-1,3-butadiyne (3) was obtained as colorless needles (mp ca. 140 °C from diethyl ether) that polymerized 100% in 24 h at 120°C to give a black, ethanol-insoluble microcrystalline product. Crystals of 3 are tr