31189-03-4

Basic information

• Product Name: Phenol, 2-(hexyloxy)-
• Synonyms: O-Hexyl-brenzcatechin;2-Hydroxy-1-hexyloxy-benzol;2-Hexyloxy-phenol;Brenzcatechinmonohexylaether
• CAS NO: 31189-03-4
• Molecular Formula: C12H18O2
• Molecular Weight: 194.274
• Mol File: 31189-03-4.mol
• Article Data: 51

Chemical Properties

• CAS DataBase Reference: Phenol, 2-(hexyloxy)-(CAS DataBase Reference)
• NIST Chemistry Reference: Phenol, 2-(hexyloxy)-(31189-03-4)
• EPA Substance Registry System: Phenol, 2-(hexyloxy)-(31189-03-4)

Safety Data

• Hazardous Substances Data: 31189-03-4(Hazardous Substances Data)

Upstream product

• 3839-35-8 4-methylbenzenesulfonic acid n-hexylester 
• 34789-97-4 pyrocatechol monosodium salt 
• 111-25-1 1-bromo-hexane 
• 120-80-9 benzene-1,2-diol 

Relevant articles and documents

Competition and promotion between two different liquid-crystalline building blocks: Mesogen-jacketed liquid-crystalline polymers and triphenylene discotic liquid crystals

Mesogen-jacketed liquid-crystalline polymers (MJLCPs) containing two triphenylene (Tp) units in the side chains, denoted as PPnV (n = 3 or 6, which is the number of the methylene units between the terephthalate core and Tp moieties in the side chains), were synthesized through conventional free radical polymerization, and the phase behaviors of these new combined main-chain/side-chain liquid-crystalline (LC) polymers were investigated. The chemical structures of the monomers were confirmed by elemental analysis, high-resolution mass spectrometry, and 1H/13C NMR. The molecular characterizations of the polymers were performed with 1H NMR, gel permeation chromatography, and thermogravimetric analysis. LC behaviors of the polymers were investigated by differential scanning calorimetry (DSC), polarized light microscopy, and wide-angle X-ray diffraction (WAXD). Both polymers exhibit excellent thermal stabilities. DSC and WAXD results indicate that covalently incorporating Tp discotic liquid crystals has a tremendous effect on the LC behaviors of MJLCPs. As expected, the glass-transition temperature decreases as the spacer length increases. Both polymers form rectangular columnar (φR) phases at relatively high temperatures. At low temperatures, however, Tp moieties in the side chains form a discotic nematic (ND) phase in conjunction with the IR phase developed by the rod-like supramolecular mesogen - the MJLCP chain as a whole, owing to the self-organization of the Tp moieties. For PP6V in particular, a higher symmetry hexagonal columnar (φH) phase forms when temperature exceeds 225 °C. Individual ordered structures developed by these two LC building blocks are not only competitive but also promotive to each other.

Synthesis and phase behavior of mesogen-jacketed liquid crystalline polymer with triphenylene discotic liquid crystal mesogen unit in side chains

A novel mesogen-jacketed liquid crystalline polymer (MJLCP) containing two triphenylene (Tp) units in the side chains, named poly[bis(3,6,7,10,11-pentakis(hexyloxy)triphenylen-2-yl)2-vinyl terephthalate] (PBTCS), was designed and successfully synthesized via conventional free radical polymerization. The chemical structure of the monomer was confirmed by 1H/13C NMR and high-resolution mass spectrometry. The molecular characterization of the polymer was performed with 1H NMR, gel permeation chromatography (GPC) and thermogravimetric analysis (TGA). The phase structure and transition of the polymer were investigated by the combination of techniques, including differential scanning calorimetry (DSC), polarizing optical microscope (POM), 1D/2D wide-angle X-ray diffraction (1D and 2D WAXD) and 1D small-angle X-ray scattering (1D SAXS). The results showed that the PBTCS reached a relatively high glass transition temperature and formed a higher symmetry hexagonal columnar (ΦH) phase due to the strong coupling effect between the Tp moieties and the MJLCP main chain. This journal is

Benzophenanthrene benzoyloxy benzene bridged perylene bisimide diester synthetic method

The invention provides a benzophenanthrene benzoyloxy benzene bridged perylene bisimide diester synthetic method. A synthesis route is characterized in that 1) p-acetenyl benzoic acid is synthesized; monohydroxy pentahexyloxy benzophenanthrene is generated; a benzophenanthrene derivative containing terminal alkyne is finally prepared; 2) N-(4-iodophenyl)perylene imine dioctyl phthalate diester is generated; and 3) an intermediate obtained by the above two parts, and a benzophenanthrene benzoyloxy benzene bridged perylene bisimide diester binary compound is obtained through a reaction by a Sonogashira cross-coupling reaction. The benzophenanthrene and its derivative are most widely discotic liquid crystal material in the prior art, have good photoelectric property, and can easily form a cylindrical liquid crystalline phase, a perylene imide derivative has strong electronic capacity, has high electronic affinity, has strong absorption capacity at a visible light zone, and is an excellent n-type organic semiconductor material. The discotic liquid crystal binary compound with an electron donor (D)-bridge (B)-acceptor (A) structure is designed and synthesized, and can be used for molecule devices of an organic photovoltaic material, a liquid crystal material, an organic solar energy cell, and an organic light-emitting diode.

Synthesis method of benzophenanthrene benzyloxy-alkyne biphenyl and propyzamide bridged perylene imide dihexyl ester

The invention aims to provide a synthesis method of benzophenanthrene benzyloxy-alkyne biphenyl and propyzamide bridged perylene imide dihexyl ester. A synthetic route is that in the first part, monohydroxyl pentahexyloxy benzophenanthrene is firstly synt