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3'-{4-[4-(3,7-dimethyloctyloxy)benzoyloxy]benzoyloxy}-4-{4-[4-[6-(1,1,3,3,5,5,5-heptamethyltrisiloxan-1yl)hex-1-yloxy]benzoyloxy]benzoyloxy}biphenyl is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1395237-87-2

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1395237-87-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1395237-87-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,9,5,2,3 and 7 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1395237-87:
(9*1)+(8*3)+(7*9)+(6*5)+(5*2)+(4*3)+(3*7)+(2*8)+(1*7)=192
192 % 10 = 2
So 1395237-87-2 is a valid CAS Registry Number.

1395237-87-2Downstream Products

1395237-87-2Relevant academic research and scientific papers

The role of temperature on dielectric relaxation and conductivity mechanism of dark conglomerate liquid crystal phase

Yildiz, Alptekin,Canli, Nimet Yilmaz,?zdemir, Zeynep Güven,Ocak, Hale,Eran, BelkIz Bilgin,Okutan, Mustafa

, p. 21 - 28 (2016)

In this study, dielectric properties and ac conductivity mechanism of the bent-core liquid crystal 3′-{4-[4-(3,7-Dimethyloctyloxy)benzoyloxy]benzoyloxy}-4-{4-[4-[6-(1,1,3,3,5,5,5-heptamethyltrisiloxan-1yl)hex-1-yloxy]benzoyloxy]benzoyloxy}biphenyl (DBB) have been analyzed by impedance spectroscopy measurements at different temperatures. According to the polarizing microscopy results, DBB liquid crystal compound exhibits a dark conglomerate mesophase (DC[?] phase) which can be identified by the occurrence of a conglomerate of domains with opposite chirality. The chiral domains of this low-birefringent mesophase become more visible by rotating the polarizer. The variation of the real (ε′) and imaginary (ε″) parts of dielectric constant with angular frequency and Cole-Cole curves of DBB have been analyzed. The fitting results for dispersion curves at different temperatures revealed that DBB system exhibits nearly Debye-type relaxation except for 125 °C. Moreover, it has been determined that while the relaxation frequencies shift to higher frequencies as the temperature increases from 25 °C to 125 °C, the peak intensities remarkably decrease with increasing temperature. According to Cole-Cole plot and phase angle versus frequency curve, it has been determined that DBB LC may have a possibility of utilizing as a super-capacitor at room temperature. Furthermore, it has been found that the conductivity mechanism of the DBB alters from Correlated Barrier Hoping (CBH) model to Quantum Tunneling Model (QMT) with in increasing temperature at high frequency region. In terms of CBH model, optical band gaps at 25 °C and 75 °C temperatures have also been calculated. Finally, activation energies for some selected angular frequencies have also been calculated.

Effects of molecular chirality on superstructural chirality in liquid crystalline dark conglomerate phases

Ocak, Hale,Bilgin-Eran, Belkiz,Prehm, Marko,Tschierske, Carsten

scheme or table, p. 7773 - 7783 (2012/09/22)

The first examples of polyphilic bent-core compounds consisting of a biphenyl central core, a chiral terminal chain and an oligo(dimethylsiloxane) end group at the other terminus have been synthesized and characterized. The mesomorphic behaviour of the compounds was investigated by differential scanning calorimetry, optical polarizing microscopy, X-ray diffraction and electro-optic methods. The olefinic precursors show monotropic or enantiotropic B1 type mesophases. The siloxane substituted analogues containing a racemic chain exhibit dark conglomerate phases (DC[*] phases) which are composed of chiral domains with opposite chirality, whereas the siloxane derivatives with a homogeneously chiral moiety show "dark enantiomer" phases (DE* phases) with uniform chirality. Under electric fields, different types of ferroelectric switching (FE) smectic and modulated smectic phases were induced. The effects of chain branching, spacer length and molecular chirality on the stability of the DCFE [*] and DEFE* phases and on the field-induced smectic and modulated smectic phases were investigated. The Royal Society of Chemistry 2012.

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