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1072193-10-2

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1072193-10-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1072193-10-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,7,2,1,9 and 3 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1072193-10:
(9*1)+(8*0)+(7*7)+(6*2)+(5*1)+(4*9)+(3*3)+(2*1)+(1*0)=122
122 % 10 = 2
So 1072193-10-2 is a valid CAS Registry Number.

1072193-10-2Downstream Products

1072193-10-2Relevant academic research and scientific papers

Achiral bent-core molecules with a series of linear or branched carbosilane termini: Dark conglomerate phases, supramolecular chirality and macroscopic polar order

Zhang, Yongqiang,Baumeister, Ute,Tschierske, Carsten,O'Callaghan, Michael J.,Walker, Christopher

, p. 2869 - 2884 (2011/11/14)

New organic-inorganic hybrid materials that combine a bent π-conjugated aromatic core with one linear or branched carbosilane unit have been synthesized and investigated, with respect to their self-assembly in liquid crystalline (LC) phases, by means of polarizing microscopy, differential scanning calorimetry (DSC), X-ray diffraction (XRD), and electro-optical techniques. Most of these achiral compounds show spontaneous symmetry breaking into chiral superstructures that represent conglomerates with macroscopic domains of opposite handedness. These fluid chiral superstructures can be frozen into the glassy state and, for one of the compounds, chirality was switched under the application of a special waveform of an applied external electric field between two enantiomeric states. This flipping of supramolecular chirality occurs between oppositely tilted structures, which represents a new mode of chirality switching. Besides spontaneous chirality, these materials show polar order, leading to ferroelectric (FE) and antiferroelectric (AF) switching modes. For one compound with a highly branched carbosilane unit, a temperature-, voltage-, and frequency-dependent reversible transition from AF switching with inversion of chirality to FE switching with retention of chirality was observed. Models were developed to explain the experimental observations, based on enthalpic and entropic contributions of distinct supermolecular arrangements in these soft matter systems.

Bent-core mesogens with branched carbosilane termini: Flipping suprastructural chirality without reversing polarity

Zhang, Yongqiang,O'Callaghan, Michael J.,Baumeister, Ute,Tschierske, Carsten

supporting information; experimental part, p. 6892 - 6896 (2009/04/06)

(Figure Presented) Back flip: Field-induced transformations between the two homogeneously chiral enantiomers of a bent-core mesogen (see picture) take place by two different mechanisms (A and B). Their combination leads to an unexpected field-induced chirality flipping (C) between the oppositely tilted structures without polarity reversal.

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