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4'-N-Decyloxybiphenyl-4-carboxylic acid, a chemical compound with the molecular formula C20H26O3, is a derivative of biphenyl and carboxylic acid featuring a decyloxy group attached to the fourth position of the biphenyl ring. 4'-N-DECYLOXYBIPHENYL-4-CARBOXYLIC ACID is known for its unique chemical structure and versatile properties, making it a valuable component in various scientific and industrial applications.

69367-32-4

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69367-32-4 Usage

Uses

Used in Liquid Crystal Research and Organic Synthesis:
4'-N-Decyloxybiphenyl-4-carboxylic acid is utilized as a key component in liquid crystal research and organic synthesis due to its mesomorphic properties. It serves as a building block for the development of liquid crystal display materials, contributing to advancements in display technology.
Used in Materials Science:
In the field of materials science, 4'-N-Decyloxybiphenyl-4-carboxylic acid plays a significant role as a precursor in the synthesis of various biologically active molecules and pharmaceuticals. Its unique structure and properties make it a promising candidate for creating new materials with specific characteristics and applications.
Used in Pharmaceutical Industry:
4'-N-Decyloxybiphenyl-4-carboxylic acid is used as a building block in the pharmaceutical industry for the synthesis of biologically active molecules. Its versatile chemical properties allow for the development of new drugs and therapeutic agents, potentially leading to breakthroughs in medicine and healthcare.

Check Digit Verification of cas no

The CAS Registry Mumber 69367-32-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,3,6 and 7 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 69367-32:
(7*6)+(6*9)+(5*3)+(4*6)+(3*7)+(2*3)+(1*2)=164
164 % 10 = 4
So 69367-32-4 is a valid CAS Registry Number.

69367-32-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 4'-Decyloxybiphenyl-4-carboxylic Acid

1.2 Other means of identification

Product number -
Other names 4-(4-decoxyphenyl)benzoic acid

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:69367-32-4 SDS

69367-32-4Relevant articles and documents

Synthesis, Fourier transform infrared, 1D and 2D NMR spectral studies on the conformation of two new cholesteryl 4-alkoxyphenyl-4′ benzoates

Yeap, Guan-Yeow,Ha, Sie-Tiong,Ito, Masato M.,Boey, Peng-Lim,Mahmood, Wan Ahmad Kamil

, p. 57 - 64 (2004)

Two new cholesteryl 4-alkoxyphenyl-4′-benzoates (CnH 2n+1OC6H4C6H4COOCh), where Ch represents cholesteryl moiety and n = 10 and 16) have been synthesized and their molecular orientation at ambient temperature were studied. The structure determination on these compounds was performed in solid state by infrared spectroscopy based on vibrational analysis wherein the cholesteryl-phenyl and phenyl-aliphatic carbon linkages were concluded. Their molecular structures were further ascertained through the 1H and 13C NMR spectra along with two-dimensional COSY, NOESY, ROESY, 1H-13C HMQC and HMBC. The long-range connectivity as concluded from the NOESY, ROESY and HMBC spectra together with the related data led to a postulation that the title compounds in the liquid state exist in the conformation whereby the cholesteryl moiety was not lying along the entire molecular long axis. The cholesteryl fragment was presumed to be bent at the ester linkage of O=C-O and the phenyl rings located between cholesteryl and alkoxy chain group are not coplanar.

Investigation of thermodynamic properties of 4-decyloxybiphenyl-4′-carboxylic acid liquid crystal and preparation of polymer dispersed liquid crystal composite

?ztürk, Emine,Ocak, Hale,Cakar, Fatih,Karanl?k, Gürkan,Cankurtaran, ?zlem,Bilgin-Eran, Belkis

, p. 24 - 30 (2018)

In this study, firstly, retention behavior of solvents on the liquid crystalline material 4-decyloxybiphenyl-4′-carboxylic acid (DBCA) has been studied by inverse gas chromatography (IGC) technique. Liquid crystal (LC) selectivity was investigated using t

Anisotropic and magnetic properties in non-metal and non-radical organic aggregates of tri-substituted phenyl derivatives

Tun Nur Iskandar, Nur Amanina Juniasari,Guan-Yeow, Yeap,Maeta, Nobuyuki,Ito, Masato M.,Nakamura, Yoshiyuki,Gas, Katarzyna,Sawicki, Maciej

, p. 210 - 217 (2019/12/25)

A new series of tri-substituted phenyl derivatives containing an aromatic imine unit and biphenyl ester possessing various numbers of carbon atoms at the terminal alkoxy chain, OCnH2n+1 (n = 7-12), along with a lateral o-ethoxy substituent have been successfully prepared and characterised by CHN microanalysis along with spectroscopic techniques (FTIR, 1H- and 13C-NMR). The texture observation under polarized light revealed that all the soft condensed materials exhibited an enantiotropic nematic (N) phase. The current studies have shown that the mesomorphic behaviour is greatly influenced by the length of the alkoxy chains wherein the thermal stability of a tri-substituted phenyl derivative will decrease if the terminal alkoxy chain is increased from n = 7 to 12. For the first time, these materials which do not possess any magnetic species in their structure, demonstrate magnetic interaction through naked eye observation as well as quantitative measurement using a SQUID magnetometer.

A modulated helical nanofilament phase

Tsai, Ethan,Richardson, Jacqueline M.,Korblova, Eva,Nakata, Michi,Chen, Dong,Shen, Yongqiang,Shao, Renfan,Clark, Noel A.,Walba, David M.

, p. 5254 - 5257 (2013/06/05)

A new liquid crystal phase, denoted modulated helical nanofilament (HNF(mod)), is formed from a very simple class of biphenyl carboxylates lacking the benzylidene aniline moieties typically found in HNF mesogens. The HNF(mod) phase represents a novel kind of nanoparticle possessing stacked aromatic rings, with potential applications in organic electronics. Copyright

Photo and electrically switchable B7 mesophase exhibiting asymmetric bent-core liquid crystals

Srinivasan, Murugesan Vijay,Kannan, Palaninathan,Roy, Arun

, p. 1584 - 1590 (2013/06/04)

The first bent-core liquid crystal materials with a photo-active azo linkage exhibiting the B7 mesophase are reported. The lower homologues of the bent-core compounds display the B1 phase and higher homologues show the B7 mesophase. The mesomorphic properties were characterized using polarized optical microscopy, differential scanning calorimetry and X-ray diffraction. The B7 phase of these materials establishes ferroelectric switching characteristics with anticlinic organization (SmCAPF) of the molecules in the layers. The bent-core molecules with an azo linkage are important for photoisomerization studies, which indicate trans to cis isomerization at 30 s, whereas the reverse processes take place over 40 s in chloroform.

Liquid crystal compounds, mixtures and devices

-

Page column 21, (2008/06/13)

An electroclinic device having two spaced cell walls each bearing electrode structures and treated on at least one facing surface with an alignment layer, a layer of a smectic liquid crystal material enclosed between the cell walls, where the liquid crystal material contains one or more of the compounds described by formula I as defined in the specification.

Liquid crystal compounds, mixtures and devices

-

, (2008/06/13)

An electoclinic device having two spaced cell walls each bearing electrode structures and treated on at least one facing surface with an alignment layer, a layer of a smectic liquid crystal material enclosed between the cell walls, where the liquid crystal material contains one or more of the compounds described by formula I as defined in the specification.

Mesomorphic trigonal bipyramidal iron(0) isocyanide complexes

Coco, Silverio,Espinet, Pablo,Marcos, Eva

, p. 1297 - 1302 (2007/10/03)

The synthesis, characterization and mesomorphic properties of three series of isocyanides and their trigonal bipyramidal iron(0) complexes [Fe(CO)4(CNR)] (R= C6H4O(O)CC6H4C6H4OC(n)H2(n)+1, C6H4C(O)OC6H4C6H4OC(n)H2(n)+1, C6H4C6H4O(O)CC6H4OC(n)H2(n)+1, n = 6, 8, 10, 12) are described. The free isocyanides exhibit nematic and/or smectic A phases for shorter chains (n = 6, 8) and only smectic A phases for longer chains, except the isocyanides CNC6H4O(O)CC6H4C6H4OC(n)H2(n)+1 which melt with extensive decomposition and do not produce mesophases. Their coordination to give the iron complexes [Fe(CO)4(CNR)] produces a slight decrease of their transition temperatures. The iron isocyanide complexes prepared show only a smectic C phase. The relationship between the molecular structure of the complexes and their thermal behaviour is discussed.

Carboxylate compounds, liquid crystal materials liquid crystal compositions and liquid crystal elements

-

, (2008/06/13)

There is provided a carboxylic acid compound represented by the following formulae (I) to (IV): STR1 a liquid crystal material consisting of the carboxylic acid ester compound, a liquid crystal composition comprising the carboxylic acid ester compound, and a liquid crystal element using the carboxylic acid ester compound. There can be obtained advantages such as low operating temperature, high speed switching, very small electric power consumption, and high-stable contrast.

Synthesis and characterization of ferroelectric and antiferroelectric liquid crystals derived from (2S)-2-(6-hydroxy-2-naphthyl)propionic acid

Wu,Chen,Chen,Wang,Shy,Hsiue

, p. 39 - 50 (2007/10/02)

A new series of chiral materials, hexyl(2s)-2-(6-(-4-(4′-alkoxyphenyl)benzoyloxy)-2′-naphthyl) propionates (HmPBNP; m = 6-18) had been prepared and their liquid crystalline properties were investigated as a function of alkyl chain length. These chiral materials exhibited novel ferroelectric Sc* and antiferroelectric ScA* phases and a propensity to the formation of the ScA* phase was found at longer alkyl chain lengths (m = 10, 12-18). An odd-even effect of the threshold voltage as a function of alkyl chain length for compounds HmPBNP (m = 12-16) possessing antiferroelectricity was observed. Spontaneous polarization and transverse dipole moment were also measured and are discussed in terms of the elongated alkyl chain length.

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