370564-68-4

Basic information

• Product Name: Benzoic acid, 3,5-bis(hexadecyloxy)-, methyl ester
• CAS NO: 370564-68-4
• Molecular Formula: C40H72O4
• Molecular Weight: 617.009
• Mol File: 370564-68-4.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: Benzoic acid, 3,5-bis(hexadecyloxy)-, methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Benzoic acid, 3,5-bis(hexadecyloxy)-, methyl ester(370564-68-4)
• EPA Substance Registry System: Benzoic acid, 3,5-bis(hexadecyloxy)-, methyl ester(370564-68-4)

Safety Data

• Hazardous Substances Data: 370564-68-4(Hazardous Substances Data)

Upstream product

• 2150-44-9 1-carbomethoxy-3,5-dihydroxybenzene 
• 112-82-3 hexadecanyl bromide 
• 99-10-5 3,5-Dihydroxybenzoic acid 
• 67-56-1 methanol 
• 503306-35-2 hexadecyl 3,5-bis(hexadecyloxy)benzoate 

Downstream Products

• 1331827-08-7 3,5-bis(3,5-bis(hexadecyloxy)benzyloxy)benzoic acid 
• 370564-71-9 methyl 3,5-bis(3,5-bis(hexadecyloxy)benzyloxy)benzoate 
• 1331827-07-6 4-(2-ethynylphenyl)but-3-ynyl 3,5-bis(hexadecyloxy)benzoate 
• 370564-69-5 1-(bromomethyl)-3,5-bis(hexadecyloxy)benzene 
• 503306-47-6 N-[O-(2,3,4,6-tetra-O-benzoyl-α-D-mannopyranosyl)oxyethyl]-3,5-bis(hexadecyloxy)benzamide 
• 41696-89-3 3,5-dihexadecyloxybenzoic acid chloride 
• 462660-44-2 ethyl 3,5-bis(3,5-dihexadecyloxybenzoylamino)-4-methyl benzoate 
• 748799-87-3 3,5-bis(3,5-dihexadecyloxybenzoylamino)-4-methyl benzoic acid 
• 308349-86-2 3,5-bis(hexadecyloxy)benzoic acid 
• 503306-39-6 N-(2-hydroxyethyl)-3,5-bis(hexadecyloxy)benzamide 

Relevant articles and documents

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.

Impact of substitution pattern and chain length on the thermotropic properties of alkoxy-substituted triphenyl-tristriazolotriazines

Tristriazolotriazines (TTTs) with a threefold alkoxyphenyl substitution were prepared and studied by DSC, polarized optical microscopy (POM) and X-ray scattering. Six pentyloxy chains are sufficient to induce liquid-crystalline behavior in these star-shap

Covalent surface functionalization of multiwalled carbon nanotubes through bergman cyclization of enediyne-containing dendrimers

A method for covalent functionalization of multiwalled carbon nanotubes (MWCNTs) was developed using the free radicals generated through Bergman cyclization of enediyne-containing compounds. Four enediyne-bearing Frechet type dendrimers were synthesized in good quantities and characterized. Then, the enediyne-containing molecules were reacted with MWCNTs in N-methyl-2- pyrrolidinone at 206 °C under nitrogen. The structure and morphology of the resulting products were characterized by thermogravimetric analysis, ultraviolet-visible spectroscopy, Fourier transform infrared spectroscopy, Raman spectroscopy, and transmission electron microscopy. The dendrimer- functionalized MWCNTs showed good solubility/dispersibility in common organic solvents and polymer solutions. They were used in the formation of polymer composites through electrospinning with polycaprolactone. The results confirmed the surface functionalization of MWCNTs.