308349-86-2

Basic information

• Product Name: Benzoic acid, 3,5-bis(hexadecyloxy)-
• CAS NO: 308349-86-2
• Molecular Formula: C39H70O4
• Molecular Weight: 602.982
• Mol File: 308349-86-2.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: Benzoic acid, 3,5-bis(hexadecyloxy)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzoic acid, 3,5-bis(hexadecyloxy)-(308349-86-2)
• EPA Substance Registry System: Benzoic acid, 3,5-bis(hexadecyloxy)-(308349-86-2)

Safety Data

• Hazardous Substances Data: 308349-86-2(Hazardous Substances Data)

Upstream product

• 370564-68-4 methyl 3,5-bis(hexadecyloxy)benzoate 
• 99-10-5 3,5-Dihydroxybenzoic acid 
• 112-82-3 hexadecanyl bromide 
• 2150-44-9 1-carbomethoxy-3,5-dihydroxybenzene 

Downstream Products

• 858363-17-4 3,5-bis-hexadecyloxy-N-[1,2,4]triazol-4-yl-benzamide 
• 1331827-07-6 4-(2-ethynylphenyl)but-3-ynyl 3,5-bis(hexadecyloxy)benzoate 
• 1331827-06-5 4-(2-(2-(trimethylsilyl)ethynyl)phenyl)but-3-ynyl 3,5-bis(hexadecyloxy)benzoate 
• 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 

Relevant articles and documents

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.

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