183151-57-7

Upstream product

• 623-24-5 1,4-bis(bromomethyl)benzene 
• 111-46-6 diethylene glycol 

Downstream Products

• 881890-43-3 2-(2-{4-[2-(2-tosyloxyethoxy)ethoxymethyl]benzyloxy}ethoxy)ethyl toluene-4-sulfonate 
• 1599475-95-2 C₃₇H₅₁N₃O₃*C₂₃H₃₁NO₆ 
• 1599475-96-3 C₃₂H₄₈N₂O₂*C₂₃H₃₁NO₆ 
• 881890-44-4 2-[2-(4-{2-[2-(2,6-dimethyl-4-tritylphenoxy)ethoxy]ethoxymethyl}benzyloxy)ethoxy]ethyl toluene-4-sulfonate 
• 881890-46-6 2-{2-[2-(4-{2-[2-(4-bromobut-2-ynyloxy)ethoxy]ethoxymethyl}benzyloxy)ethoxy]ethoxy}-1,3-dimethyl-5-tritylbenzol 
• 881890-45-5 4-{2-[2-(4-{2-[2-(2,6-dimethyl-4-tritylphenoxy)ethoxy]ethoxymethyl}benzyloxy)ethoxy]ethoxy}but-2-yn-1-ol 

Relevant academic research and scientific papers

Effects of side arm length and structure of para-substituted phenyl derivatives on their binding to the host cyclobis(paraquat-p-phenylene)

The binding constants with the host cyclobis(paraquat-p-phenylene), 14+, have been determined in CH3CN by UV-vis spectrophotometry for a series of p-phenylene guests, symmetrically substituted with side arms of varying length and fun

Five additional macrocycles that allow Na+ ion-templated threading of guest units featuring a single urea or amide functionality

Five analogues of the macrocycle BPX26C6 are also capable of recognizing single urea and/or amide functionalities in the presence of templating Na + ions. We have unambiguously confirmed the formation of such [2]pseudorotaxane complexes in solution through syntheses of the corresponding [2]rotaxanes. This journal is the Partner Organisations 2014.