462660-44-2

Basic information

• Product Name: Benzoic acid, 3,5-bis[[3,5-bis(hexadecyloxy)benzoyl]amino]-4-methyl-, ethyl ester
• CAS NO: 462660-44-2
• Molecular Formula: C88H150N2O8
• Molecular Weight: 1364.17
• Mol File: 462660-44-2.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Benzoic acid, 3,5-bis[[3,5-bis(hexadecyloxy)benzoyl]amino]-4-methyl-, ethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Benzoic acid, 3,5-bis[[3,5-bis(hexadecyloxy)benzoyl]amino]-4-methyl-, ethyl ester(462660-44-2)
• EPA Substance Registry System: Benzoic acid, 3,5-bis[[3,5-bis(hexadecyloxy)benzoyl]amino]-4-methyl-, ethyl ester(462660-44-2)

Safety Data

• Hazardous Substances Data: 462660-44-2(Hazardous Substances Data)

Upstream product

• 2150-44-9 1-carbomethoxy-3,5-dihydroxybenzene 
• 16533-71-4 3,5-dinitro-p-toluic acid 
• 5400-86-2 ethyl 3,5-dinitro-4-methylbenzoate 
• 6633-36-9 3,5-diamino-4-methylbenzoic acid 
• 308349-86-2 3,5-bis(hexadecyloxy)benzoic acid 
• 370564-68-4 methyl 3,5-bis(hexadecyloxy)benzoate 
• 112-82-3 hexadecanyl bromide 
• 42908-12-3 3,5-diamino-4-methyl benzoic acid ethyl ester 
• 41696-89-3 3,5-dihexadecyloxybenzoic acid chloride 

Downstream Products

• 748799-87-3 3,5-bis(3,5-dihexadecyloxybenzoylamino)-4-methyl benzoic acid 

Relevant articles and documents

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

A convenient protocol for the synthesis of ligands from a 4-methyl-3,5-diacylaminophenyl platform

The synthesis of stable and highly organized phenanthroline, terpyridine, and pyridino-oxazoline ligands bearing one or two 4-methyl-3,5-diacylaminophenyl modules equipped with two lateral dialkoxyphenyl groups has been performed using EDC·HCl and DMAP reagents in the final coupling reaction. Evidently, in the final ligands and in the solid state intermolecular hydrogen bonding maintains the coherence of the tridimensional structure as clearly evidenced by FT-IR and X-ray diffraction spectroscopy in the cases of the methoxy ligands. The supramolecular packing is also maintained by additional π-π stacking interactions.