Category: 50670-76-3

Faya, V. published the artcileS_C^* and S_C̃^_* phases in chiral non-symmetric dimesogens, Application of Ethyl 4′-hydroxy-[1,1′-biphenyl]-4-carboxylate, the publication is Liquid Crystals (1996), 21(4), 485-503, database is CAplus.

The authors synthesized two sep. homologous series of chiral nonsym. dimesogens: these have a two Ph ring moiety bearing a terminal alkoxy chain linked via a methylenic spacer to a chiral three Ph ring mesogen which itself displays antiferroelec. properties. Depending on the parity of the number of carbons constituting the spacer, two kinds of mesomorphic behavior were found. When the spacer is even, various S_C^* phases (S_C^*A,S_C^*FI,S_C^*,S_C^*α) were identified without doubt, whereas when the spacer is odd, a tilted modulated phase (S_C̃^*) was observed and characterized. In each case, the authors study the effect of the length of the alkoxy chain at the end of the shorter moiety. The alternation of the mesomorphic behavior with the spacer parity was interpreted in terms of mol. shape, but the authors have also discussed the influence of some chem. parameters on the stability of the S_C^*A phase.

Liquid Crystals published new progress about 50670-76-3. 50670-76-3 belongs to esters-buliding-blocks, auxiliary class Benzene,Phenol,Ester, name is Ethyl 4′-hydroxy-[1,1′-biphenyl]-4-carboxylate, and the molecular formula is C15H14O3, Application of Ethyl 4′-hydroxy-[1,1′-biphenyl]-4-carboxylate.

Referemce:
https://en.wikipedia.org/wiki/Ester,
Ester – an overview | ScienceDirect Topics

Loudet, J. C. published the artcileColloidal Structures from Bulk Demixing in Liquid Crystals, COA of Formula: C15H14O3, the publication is Langmuir (2004), 20(26), 11336-11347, database is CAplus and MEDLINE.

This exptl. paper deals with phase separations of binary mixtures composed of a continuous liquid crystal phase and an isotropic dispersed phase. In contrast to isotropic binary mixtures, the studied mixtures do not lead to a full phase separation but to a self-ordering of colloidal particles, as reported earlier (Loudet, J. C. et al., Nature 2000, 407, 611). The authors present here further aspects of such phase separations which include the kinetics of the phase separation, the origin of the formation of dislocation-like patterns, the influence of surfactants, chiral additives, and temperature on the formed colloidal structures. (i) The dislocations in chain arrays can be seen as kinetically frozen defects, (ii) temperature can be used to control the size of the domains formed upon demixing, (iii) a slight change in surface chem., via the addition of surfactants, profoundly alters the formed colloidal structures, and (iv) chiral additives gave unique helical pearl chains which reflect the symmetry of the liquid crystal phase they are embedded in.

Langmuir published new progress about 50670-76-3. 50670-76-3 belongs to esters-buliding-blocks, auxiliary class Benzene,Phenol,Ester, name is Ethyl 4′-hydroxy-[1,1′-biphenyl]-4-carboxylate, and the molecular formula is C15H14O3, COA of Formula: C15H14O3.

Referemce:
https://en.wikipedia.org/wiki/Ester,
Ester – an overview | ScienceDirect Topics

Saliner, Ana Gallegos published the artcileMolecular Quantum Similarity Analysis of Estrogenic Activity, Formula: C15H14O3, the publication is Journal of Chemical Information and Computer Sciences (2003), 43(4), 1166-1176, database is CAplus and MEDLINE.

The main objective of this study was to evaluate the capability of 120 aromatic chems. to bind to the human alpha estrogen receptor (hERα) by the use of quantum similarity methods. The exptl. data were segregated into two categories, i.e., those compounds with and without estrogenicity activity (active and inactive). To identify potential ligands, semiquant. structure-activity relationships were developed for the complete set correlating the presence or lack of binding affinity to the estrogen receptor with structural features of the mols. The structure-activity relationships were based upon mol. similarity indexes, which implicitly contain information related to changes in the electron distributions of the mols., along with indicator variables, accounting for several structural features. In addition, the whole set was split into several chem. classes for modeling purposes. Models were validated by dividing the complete set into several training and test sets to allow for external predictions to be made.

Journal of Chemical Information and Computer Sciences published new progress about 50670-76-3. 50670-76-3 belongs to esters-buliding-blocks, auxiliary class Benzene,Phenol,Ester, name is Ethyl 4′-hydroxy-[1,1′-biphenyl]-4-carboxylate, and the molecular formula is C15H14O3, Formula: C15H14O3.

Referemce:
https://en.wikipedia.org/wiki/Ester,
Ester – an overview | ScienceDirect Topics