710338-34-4

Upstream product

• 71186-67-9 3,4-diallyloxybenzaldehyde 
• 139-85-5 3,4-dihydroxybenzaldehyde 
• 52507-49-0 4-hydroxy-3-(2-propenyloxy)benzaldehyde 
• 756525-88-9 3-allyloxy-4-hydroxybenzyl alcohol 
• 106-93-4 ethylene dibromide 

Downstream Products

• 391895-30-0 {3-allyloxy-4-[2-(3,8,13-trimethoxy-7,12-bis-{2-[2-methoxy-4-(tetrahydro-pyran-2-yloxymethyl)-phenoxy]-ethoxy}-10,15-dihydro-5H-tribenzo[a,d,g]cyclononen-2-yloxy)-ethoxy]-phenyl}-methanol 
• 710338-31-1 [4-(2-{7-{2-[2-allyloxy-4-(tetrahydropyran-2-yloxymethyl)phenoxy]ethoxy}-12-[2-(4-hydroxymethyl-2-methoxyphenoxy)ethoxy]-3,8,13-trimethoxy-10,15-dihydro-5H-tribenzo[a,d,g]cyclononen-2-yloxy}ethoxy)-3-methoxyphenyl]methanol 
• 710338-27-5 2-[3-allyloxy-4-(2-iodoethoxy)benzyloxy]tetrahydropyran 
• 426821-81-0 [3-allyloxy-4-(2-iodoethoxy)phenyl]methanol 

Relevant academic research and scientific papers

Enantiopure C1-Cyclotriveratrylene with a Reversed Spatial Arrangement of the Substituents

Cyclotriveratrylene (CTV) is a macrocyclic cyclophane presenting a bowl-shaped conformation, used as building block to construct cryptophane and hemicryptophane capsules. A method to synthesize new enantiopure CTV derivatives with an unprecedented spatial

Synthesis and application of cryptophanol hosts: 129Xe NMR spectroscopy of a deuterium-labeled (Xe)2@bis-cryptophane complex

The new bis-cryptophanes 7-9 were prepared from cryptophanols 1-3 and illustrate the synthetic possibilities offered by the latter for the design of new host systems featuring the preparation of large supramolecular receptors and new polycryptophane bio-s

Development of a functionalized xenon biosensor

NMR-based biosensors that utilize laser-polarized xenon offer potential advantages beyond current sensing technologies. These advantages include the capacity to simultaneously detect multiple analytes, the applicability to in vivo spectroscopy and imaging