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CAS

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4,4'-DI-N-HEXYLOXYBIPHENYL, also known as 6O, is a chemical compound with the molecular formula C24H34O and a molecular weight of 338.52 g/mol. It is a liquid crystal material characterized by its stable mesophase and wide liquid crystalline temperature range. 4,4'-DI-N-HEXYLOXYBIPHENYL is known for its good chemical stability and compatibility with other liquid crystal materials, making it a valuable component in the fabrication of stable and high-performance liquid crystal devices.

142450-58-6

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142450-58-6 Usage

Uses

Used in Liquid Crystal Displays (LCDs):
4,4'-DI-N-HEXYLOXYBIPHENYL is used as a liquid crystal material in LCDs for its stable mesophase and wide liquid crystalline temperature range, which makes it suitable for high-temperature applications and ensures consistent performance.
Used in Optical Devices:
In the optical devices industry, 4,4'-DI-N-HEXYLOXYBIPHENYL is used as a component in the fabrication of devices that require stable and high-performance liquid crystal materials, thanks to its good chemical stability and compatibility with other liquid crystal materials.
Used in Organic Electronics:
4,4'-DI-N-HEXYLOXYBIPHENYL is utilized in organic electronics as a liquid crystal material to enhance the performance and stability of electronic devices, capitalizing on its wide temperature range and chemical stability.

Check Digit Verification of cas no

The CAS Registry Mumber 142450-58-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,2,4,5 and 0 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 142450-58:
(8*1)+(7*4)+(6*2)+(5*4)+(4*5)+(3*0)+(2*5)+(1*8)=106
106 % 10 = 6
So 142450-58-6 is a valid CAS Registry Number.

142450-58-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-hexoxy-4-(4-hexoxyphenyl)benzene

1.2 Other means of identification

Product number -
Other names 4,4'-Dihexyloxy-1,1'-biphenyl

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:142450-58-6 SDS

142450-58-6Downstream Products

142450-58-6Relevant articles and documents

Synthesis and luminescent studies of poly(phenylenevinylene)s containing a biphenyl moiety

Sarker, Ananda M.,Ding, Liming,Lahti, Paul M.,Karasz, Frank E.

, p. 223 - 230 (2002)

The polymers discussed in this contribution consist of phenylenevinylene chromophores linked together across flexible biphenyl hinges to shorten the effective conjugation length and to give sufficiently twisted structures that interchain aggregation is limited or prevented. They are poly[(2,5- dihexyloxy-p-phenylenevinylene)-alt-(4,4′-dihexyloxy-3, 3′-biphenylenevinylene)] (1), poly[(2,5-dihexyloxy- p-phenylenevinylene)-alt-(2,2′-dihexyloxy-3,3′ -biphenylenevinylene)] (2), and poly[(2,5-dihexyloxy-p- phenylenevinylene)-alt-(2,2′-biphenylenevinylene)] (3). Absorption spectra in dilute solution and solid states are very similar for 1-3, consistent with the absence of aggregation effects in their ground electronic states. Photoluminescence emission spectra showed substantial red shifts in the solid state relative to dilute solution phase spectra. Solution emission quantum yields ranged from 0.26 to 0.42. LEDs based on 1-3 gave blue-green emission with maxima in the 480-510 nm range. The similarity of the photoluminescence and electroluminescence spectra for the polymers is consistent with emission from the same or very similar excited-state species. For LEDs based upon the highest quantum efficiency photoluminescent emitter, 1, better luminance was achieved using PEDOT-PSS hole injection layers in double-layer LEDs than using PPV.

Rewritable color recording media consisting of leuco dye and biphenyl developer with a long alkyl chain

Naito, Katsuyuki

, p. 1379 - 1384 (1998)

Media formulated using two compounds (a leuco dye and 4-alkoxyl-4′-hydroxybiphenyl) were colored in the amorphous state and colorless in the crystalline state. As the alkyl chain length of the biphenyl compound increased, the contrast ratio and thermal stability of the amorphous states increased. Additionally, the crystallization velocity increased for the media with a long alkyl chain. Leuco dyes with a high glass transition temperature also produced thermally stable amorphous states. The origin of the long alkyl chain effects is discussed.

Design and synthesis of novel calamitic and discotic materials based on the photorefractive carbazole unit

Manickam,Iqbal,Spencer,Ashton,Kumar,Donovan,Preece

experimental part, p. 84 - 100 (2011/05/03)

The incorporation of photorefractive molecular units, such as carbazole, into anisotropic materials (liquid crystals) may offer many advantages over conventional electrical poling of photorefractive polymers. Thus, a series of symmetric 3,6-disubstituted

Synthesis, structure, and mesomorphic properties of liquid crystals with a bitropone core

Kubo, Kanji,Sutoh, Takanori,Mori, Akira,Ujiie, Seiji

, p. 1353 - 1358 (2007/10/03)

New troponoid liquid crystals (1-4) with a bitropone core were prepared. The ester derivatives (1) had enantiotropic smectic A and/or C phases with higher thermal stabilities than the corresponding benzenoid derivatives (5), which had a smectic B phase. T

Selective etherification of polyhydroxybenzenes using PEG 200 as solvent or cosolvent

Berdague, P.,Perez, F.,Courtieu, J.,Bayle, J. P.

, p. 475 - 480 (2007/10/02)

The monoalkylation of hydroquinone is performed using PEG 200 as a solvent or a cosolvent.The effect on the selectivity of the base strength, the temperature, and the percentage of cosolvent are discussed.The substituted phenols were found to behave differently upon etherification.When a carboxylic function is present in the ring, the hydroxybenzoic acids were selectively etherified using pure PEG and sodium hydroxyde as a base.Substituted diphenols were selectively etherified using a mixture of PEG and dioxan and potassium hydrogencarbonate as a base.Keywords - etherification / selectivity / polyhydroxybenzenes / polyethylene glycol

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