794450-49-0

Upstream product

• 118896-79-0 6-(hydroxymethyl)-6'-methyl-1,10-phenanthroline 
• 820216-69-1 3,5-bis(3,5-didodecyloxybenzoylamino)-4-methyl benzoic acid 
• 6633-36-9 3,5-diamino-4-methylbenzoic acid 
• 820216-67-9 ethyl 3,5-bis(3,5-didodecyloxybenzoylamino)-4-methyl benzoate 
• 5400-86-2 ethyl 3,5-dinitro-4-methylbenzoate 
• 16533-71-4 3,5-dinitro-p-toluic acid 
• 2150-44-9 1-carbomethoxy-3,5-dihydroxybenzene 
• 123126-38-5 3,5-bis-dodecyloxy-benzoic acid methyl ester 
• 123126-40-9 3,5-didodecyloxybenzoic acid 
• 123126-41-0 3,5-didodecyloxybenzoic acid chloride 
• 143-15-7 1-dodecylbromide 
• 42908-12-3 3,5-diamino-4-methyl benzoic acid ethyl ester 

Downstream Products

• 783372-76-9 (CH₃C₁₂H₆N₂CH₂OCOC₆H₂(CH₃)(NHCOC₆H₃(O(CH₂)11CH₃)2)2)2Cu⁽¹⁺⁾*BF₄^(1-)=C₁₆₈H₂₄₈CuN₈O₁₆BF₄ 

Relevant academic research and scientific papers

Synthesis of oligopyridinic scaffolds from amido substituted phenyl rings for extended hydrogen bonding

A series of phenanthroline, terpyridine and pyridino-oxazoline ligands combining a 4-methyl-3,5-diacylaminophenyl platform and two dialkoxyphenyl groups has been prepared by a linear multistep protocol. The synthetic potential of 4-methyl-3,5-(diacyl-amin

Tuning organogels and mesophases will phenanthroline ligands and their copper complexes by inter- to intramolecular hydrogen bonds

A novel family of highly functionalized molecules consisting of a central 4-methyl-3,5-diacylaminobenzene platform linked in close proximity to the methyl group by two lateral aromatic rings each equipped with two long alkoxy chains has been rationally de

Mesomorphic phenanthroline derivatives: Novel architectures based on hydrogen bonding

Strong hydrogen bonding has been observed in mesomorphic phenanthroline compounds engineered from diacylamino-benzene platforms: a columnar organization is found in the free ligands (n = 12 or 16) whereas a smectic arrangement is evidenced in a palladium complex (n = 16).