162456-86-2

Upstream product

• 1032106-16-3 2-(4-tritylphenoxy)acetic acid ethyl ester 
• 978-86-9 4-tritylphenol 
• 105-36-2 ethyl bromoacetate 
• 79-11-8 chloroacetic acid 
• 3926-62-3 sodium monochloroacetic acid 

Downstream Products

• 954418-73-6 ethyl 2-(2-(2-(4-tritylphenoxy)acetamido)acetamido)acetate 
• 978-86-9 4-tritylphenol 
• 1052166-37-6 N-(4-iodophenyl)-2-(2-(4-tritylphenoxy)acetamido)acetamide 
• 954418-75-8 C₅₄H₅₀N₄O₁₁ 
• 954418-74-7 2-(2-(2-(4-tritylphenoxy)acetamido)acetamido)acetic acid 

Relevant academic research and scientific papers

A photoswitchable rotaxane operating in monolayers on solid support

A novel photoswitchable rotaxane was synthesised and its switching behaviour in solution was analysed with NMR and UV-Vis. A monolayer of rotaxanes was deposited on glass surfaces and the on-surface photoswitching was investigated. Angle-resolved NEXAFS spectra revealed a preferential orientation that reversibly changes upon switching.

Synthesis and properties of [4-(triphenylmethyl)phenoxy]acetic and 3-[4-(triphenylmethyl)phenoxy]propionic acids and their condensation with phthalimide leading to meso-substituted tetrabenzoporphyrins

Condensation of 4-(triphenylmethyl)phenol with monochloroacetic and 3-bromopropionic acids gave, respectively, [4-(triphenylmethyl)phenoxy]acetic and 3-[4-(triphenylmethyl)phenoxy]propionic acids which reacted with phthalimide in the presence of zinc acet

Photoisomerization of spiropyran for driving a molecular shuttle

A novel light-powered molecular shuttle was synthesized which can switch the movement of a macrocycle between two distinct stations-dipeptide and zwitterionic ME-by exploiting the photoisomerization of spiropyran. The macrocycle resides selectively in the

Analysis of the Conformational Behaviour of Perfunctionalized β-Cyclodextrins. Part 1. Evidence for Insertion of one of the Rim Substituents into the Cyclodextrin Cavity in Organic Solvents

Several functionalized β-cyclodextrins have been shown to exhibit conformational isomerism.The analysis of the conformational behaviour of several derivatives strongly suggests that a slow exchange occurs between C7 and C1 conformers, the C1 probably invo