309758-34-7

Upstream product

• 21022-88-8 methyl 3,5-dihydroxy-4-allyloxy benzoate 
• 100-39-0 benzyl bromide 
• 99-24-1 methyl galloate 

Downstream Products

• 1026436-82-7 2-Allyloxy-1,3-bis-benzyloxy-5-chloromethyl-benzene 
• 309758-40-5 [3,5-bis-(4-allyloxy-3,5-bis-benzyloxy-benzyloxy)-phenyl]-methanol 
• 309758-36-9 3,5-bis-(4-allyloxy-3,5-bis-benzyloxy-benzyloxy)-benzoic acid methyl ester 
• 309758-41-6 [4-allyloxy-3,5-bis-(4-allyloxy-3,5-bis-benzyloxy-benzyloxy)-phenyl]-methanol 
• 309758-38-1 4-allyloxy-3,5-bis-(4-allyloxy-3,5-bis-benzyloxy-benzyloxy)-benzoic acid methyl ester 
• 1123215-07-5 methyl 3,5-bis(benzyloxy)-4-hydroxybenzoate 
• 1357284-47-9 C₃₄H₁₉Cl₂F₅N₆O₅ 
• 1357284-46-8 C₂₂H₁₁Cl₂F₅N₆O₇ 
• 1357284-45-7 C₄₈H₂₄F₁₀N₆O₁₀ 
• 1357479-96-9 C₃₆H₁₆F₁₀N₆O₁₂ 
• 1357284-41-3 C₂₈H₁₉F₅O₅ 
• 1357284-37-7 C₁₄H₇F₅O₅ 
• 309758-35-8 (4-allyloxy-3,5-bis-benzyloxy-phenyl)-methanol 

Relevant academic research and scientific papers

Synthesis and structure of oxacalix[2]arene[2]triazines of an expanded π-electron-deficient cavity and their interactions with anions

Novel macrocyclic anion receptors based on the principle of anion-π interactions were reported. By means of both post-macrocyclization modification protocol and the stepwise fragment coupling approach, functionalized oxacalix[2]arene[2]triazines bearing two other electron-deficient (hetero)aromatic rings on the lower rim were efficiently synthesized. The resulting oxacalix[2]arene[2]triazine macrocyclesadopt 1,3-alternate conformation, yielding therefore an expanded electron-deficient cavity or space consisting of two triazine rings and two appending aromatic rings. Spectroscopic titration study showed the selective interaction of the pentafluorophenyl- substituted oxacalix[2]arene[2]triazine with azide and fluoride in solution with the binding constants (K1:1) ranging from 1.33 × 10 3 to 3.52 × 103 M-1.

A simple method for controlling dendritic architecture and diversity: A parallel monomer combination approach

A novel parallel monomer combination approach to manipulating the architectural disposition of dendritic macromolecules is described. It harnesses the synthetic speed and power of the double-stage convergent growth approach and classical parallel synthesi