869358-30-5

Upstream product

• 100-20-9 terephthaloyl chloride 
• 146904-78-1 (R)-1-cyclohexylethylamine 

Downstream Products

• 869358-35-0 N,N'-dibutyl-N,N'-bis-[4-(4-iodo-2,5-dimethyl-phenylethynyl)-phenyl]-terephthalamide 
• 869358-33-8 N,N'-dibutyl-N,N'-bis-[4-(4-iodo-phenylethynyl)-phenyl]-terephthalamide 
• 869358-32-7 N,N'-dibutyl-N,N'-bis-(4-ethynyl-phenyl)-terephthalamide 
• 869358-31-6 N,N'-dibutyl-N,N'-bis-(4-trimethylsilanylethynyl-phenyl)-terephthalamide 

Relevant academic research and scientific papers

A foldable cyclic oligomer: Chiroptical modulation through molecular folding upon complexation and a change in temperature

A foldable cyclic oligomer 1 consisting of three terephthalamide units spaced with a 3-fold o-phenylene unit presented a dynamic pair of enantiomeric forms through molecular folding, to which the external chirality on a ditopic guest [(S,S)-2 or (R,R)-2]

Stereospecific change in conformation upon complexation of an exoditopic tetraamide host with a bis(ammonium) guest: Chiral recognition and strong CD signaling

Upon complexation of a rectangular-shaped achiral macrocyclic host with chiral guests, twisting deformation occurs to induce exciton-type bisignated CD, whereas a chiral rectangular host undergoes a similar structural change only with the matching enantio