794450-49-0

Upstream product

• 6633-36-9 3,5-diamino-4-methylbenzoic acid 
• 820216-67-9 ethyl 3,5-bis(3,5-didodecyloxybenzoylamino)-4-methyl benzoate 
• 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 
• 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 
• 118896-79-0 6-(hydroxymethyl)-6'-methyl-1,10-phenanthroline 
• 820216-69-1 3,5-bis(3,5-didodecyloxybenzoylamino)-4-methyl benzoic acid 

Downstream Products

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

Relevant academic research and scientific papers

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

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

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).