52244-88-9

Basic information

• Product Name: Ethanone, 1-[4-(tetradecyloxy)phenyl]-
• CAS NO: 52244-88-9
• Molecular Formula: C22H36O2
• Molecular Weight: 332.527
• Mol File: 52244-88-9.mol
• Article Data: 15

Chemical Properties

• CAS DataBase Reference: Ethanone, 1-[4-(tetradecyloxy)phenyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: Ethanone, 1-[4-(tetradecyloxy)phenyl]-(52244-88-9)
• EPA Substance Registry System: Ethanone, 1-[4-(tetradecyloxy)phenyl]-(52244-88-9)

Safety Data

• Hazardous Substances Data: 52244-88-9(Hazardous Substances Data)

Upstream product

• 108-95-2 phenol 
• 112-71-0 1-Bromotetradecane 
• 35021-69-3 tetradecyl phenyl ether 
• 108-24-7 acetic anhydride 
• 19218-94-1 1-iodotetradecane 
• 99-93-4 4-Hydroxyacetophenone 

Downstream Products

• 52244-83-4 2-<4-(Tetradecyloxy)-benzoyl>-essigsaeure-methylester 
• 154845-71-3 1,3-di(4-n-tetradecanoxyphenyl)propane-1,3-dione 
• 1198620-26-6 1-(4-tetradecyloxyphenyl)-3-hydroxy-2-propen-1-one 

Relevant articles and documents

Liquid crystal behavior, photoluminescence and gas sensing: A new series of ionic liquid crystal imidazole and benzoimidazole bearing chalcone groups, synthesis and characterization

Four new series of chalcones containing imidazole bromonium and benzimidazole bromonium salts with spacer alkyl chains (Cn, n = 2 and 4) were synthesized and the chemical structure, thermal behavior, photoluminescence and gas sensing were characterized by

Synthesis and liquid crystalline properties of a new homologous series of 4,5-disubstituted 2H-[1,2,3]-triazoles via azide-chalcone oxidative cycloaddition reaction

A new homologous series of 4,5-disubstituted 2H-[1,2,3]-triazole derivatives were synthesized from chalcones and sodium azide via oxidative cycloaddition reaction; CuI was used as catalyst. Flexibility in the synthesized molecules was provided by attaching straight alkoxy chains. The synthesized compounds were characterized by elemental analysis, and 1HNMRand 13CNMRand LC-MS spectroscopies . The stability and range of the mesophases increased with the length of the chain on the triazoles. The melting point, transition temperatures, and enantiotropic liquid crystal morphologies were determined by differential scanning calorimetry (DSC) and polarizing optical microscopy (POM) equipped with a hot stage. Journal compilation

Mechanochromic luminescent difluoroboron beta-diketonates

The invention provides luminescent solid-state compositions comprising difluoroboron beta-diketonates wherein the compositions can exhibit mechanochromic luminescence. The mechanochromic effect on the luminescence can be reversible, such as thermally reversible. Various solid-state forms of the invention can have emission spectra that differ from the properties of the respective difluoroboron beta-diketonate in solution. The mechanochromic effect can be stimulated by pressure such as handwriting, and can be reversed over a period of minutes to hours at room temperature. The invention also provides methods of making and methods of using the solid-state compositions, such as for sensors and for information displays for use in biological sensing, and in art, design, and consumer products. Compositions of the invention, such as compositions in nanoparticulate form, or contained within a matrix material, can be used in conjunction with fluorescence microscopy to provide information concerning pressures and tensions within and external to living cells, tissues, or organisms.