710338-34-4

Upstream product

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

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 
• 426821-81-0 [3-allyloxy-4-(2-iodoethoxy)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 

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

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

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