391895-30-0

Upstream product

• 86534-12-5 (±)-2,7,12-trimethoxy-3,8,13-tris(2-propenyloxy)-10,15-dihydro-5Htribenzo[a,d,g]cyclononene 
• 426821-81-0 [3-allyloxy-4-(2-iodoethoxy)phenyl]methanol 
• 811867-92-2 C₅₇H₆₈O₁₄ 
• 811867-91-1 12-allyloxy-3,8,13-trimethoxy-10,15-dihydro-5H-tribenzo[a,d,g]cyclononene-2,7-diol 
• 139-85-5 3,4-dihydroxybenzaldehyde 
• 71186-67-9 3,4-diallyloxybenzaldehyde 
• 710338-34-4 4-(2-bromoethoxy)-3-(2-propen-1-yloxy)benzenemethanol 
• 811867-93-3 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-ol 
• 347894-43-3 2-[4-(2-iodoethoxy)-3-methoxybenzyloxy]-tetrahydropyran 
• 426821-82-1 12-[2-(2-allyloxy-4-hydroxymethyl-phenoxy)-ethoxy]-3,8,13-trimethoxy-10,15-dihydro-5H-tribenzo[a,d,g]cyclononene-2,7-diol 
• 81370-49-2 cyclotriguaiacyclene 

Relevant academic research and scientific papers

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

Cryptophanols, new versatile compounds for the synthesis of functionalized cryptophanes and polycryptophanes

After deprotection with a palladium catalyst, mono-allylated cryptophane-A (1, 2) and cryptophane-E (3) gave the new cryptophanols 4, 5 and 6, respectively, which are important key compounds for the preparation of monofunctionalized cryptophanes as well a