86840-97-3

Upstream product

• 111-83-1 1-bromo-octane 
• 2150-47-2 methyl 2,4-dihydroxybenzoate 
• 89-86-1 4-hydroxysalicylic acid 
• 111-87-5 octanol 

Downstream Products

• 86840-99-5 acide 2-hydroxy-4-octyloxybenzoique 
• 41697-03-4 2-hydroxy-4-octoxy-benzhydrazide 
• 874210-24-9 methyl 2-methoxy-4-octyloxybenzoate 
• 134465-08-0 4'-(undecyloxy)biphenyl-4-yl 4-(octyloxy)-2-(pent-4-enyloxy)benzoate 
• 134465-17-1 4'-(undecyloxy)biphenyl-4-yl 4-(octyloxy)-2-(undec-10-enyloxy)benzoate 
• 1020267-82-6 4-(4-cyanophenyl)phenyl 2-hydroxy-4-octyloxybenzoate 
• 1209480-83-0 4-(4-cyanophenyl)phenyl 4-octyloxy-2-{11-{4-[2-(2-fluoro-4-hexyloxyphenyl)pyrimidin-5-yl]phenyloxy}undecanoyloxy}benzoate 
• 1209480-82-9 4-(4-cyanophenyl)phenyl 4-octyloxy-2-{11-{4-[2-(4-hexylphenyl)pyrimidin-5-yl]phenyloxy}undecanoyloxy}benzoate 
• 1209480-81-8 4-(4-cyanophenyl)phenyl 4-octyloxy-2-{11-{4-[4-(4-hexylphenyl)-2,3-difluorophenyl]phenyloxy}undecanoyloxy}benzoate 

Relevant academic research and scientific papers

SOLID FOAM COMPRISING MESOGENIC LIGAND-FUNCTIONALIZED NANOPARTICLES AND METHODS OF MAKING AND USING THE SAME

Solid foam structures having multiple compartments comprising mesogenic ligand-functionalized nanoparticles are provided. Compositions that include these structures, as well as methods of making the structures are also provided. The structures, compositions and methods find use in a variety of applications, such as, photonics, luminescent coatings and multi-compartment encapsulation technologies.

Achiral H-shaped liquid crystals exhibiting an electric-field-induced chiral nematic phase

We prepared two achiral H-shaped liquid crystals, 4,4′-bis(7-{2-[4-(4-cyanophenyl)phenyloxycarbonyl]-5-octyloxyphenyloxycarbonyl}heptyloxy)biphenyl (I) and 4,4′-bis(7-{2-[4-(4-cyanophenyl)phenyloxycarbonyl]-5-octyloxyphenyloxycarbonyl}heptyloxy)octafluoro

THREE-DIMENSIONAL STRUCTURES OF MESOGENIC LIGAND-FUNCTIONALIZED NANOPARTICLES AND METHODS OF MAKING AND USING THE SAME

Three-dimensional structures of stably associated mesogenic ligand-functionalized nanoparticles are provided. Compositions that include these structures, as well as methods of making the structures are also provided. The structures, compositions and methods find use in a variety of applications, such as light emitting devices (e.g., video displays, lights, etc.), inks, photonics and encapsulation technologies.

Structure-properties relationships in liquid crystal thiols

Two new series of thiols were studied in order to establish the structure-properties relationships. First series consists of compounds with three or four aromatic rings as rigid part of mesogen and the second contains thiols with a flexible chain attached

Structure-property relationships in non-chiral liquid crystal oligomers stabilizing blue phases

We prepared 4-(4-cyanophenyl)phenyl 4-octyloxybenzoate derivatives possessing a laterally attached mesogen and investigated their phase transition behavior. They showed a wide temperature range of a nematic phase in spite of being far from a rod-like stru

Synthesis of crescent aromatic oligoamides

This article describes the synthetic procedures for the preparation of crescent (and helical) aromatic oligoamides developed in recent years in our laboratory. The large-scale preparation of a variety of monomers derived from various tetrasubstituted benzenes is presented. Three different strategies for constructing various oligomers consisting of meta- and meta/para-linked benzene residues are discussed. Factors affecting coupling efficiency and yields are analyzed. The developed synthetic methods have provided the basis for the preparation of longer oligomers and for the development of solid-phase synthesis.

Nematic silsesquioxanes - Towards nanocrystals dispersed in a nematic liquid crystal matrix

The reaction of suitable organic groups in combination with well defined inorganic silsequioxane cores leads to covalently bound organic-inorganic hybrid materials, which exhibit nematic and smectic C phase behaviour close to room temperature.

Preparation for external application to the skin and novel benzoic acid derivatives

Disclosed is a preparation for external application to the skin characterized by containing at least one of benzoic acid derivatives represented by formula (I) or pharmacologically acceptable salts thereof as an active ingredient, the preparation having s

The Coordinative Behaviour of N-Substituted 2-(Δ2-Imidazolin-2-yl)-phenols as Metal Extractants

N-Substituted 2-(Δ2-imidazolin-2-yl)-phenols (R4NNOH) are obtained by the reaction of N-alkyl diaminoethane-1,2 and 2-hydroxybenzoic acid esters.In contrast to many other copper(II) complexes with the donor set N2O22- (A),

O- and N-Alkylsubstituted 2-(2'-Hydroxyphenyl)-benzimidazoles and -1,3,4-Oxadiazoles as Complexing and Extracting Agents for Copper-II-Ions

2-(2'-Alkoxyphenyl)-benzimidazoles 1, 1-alkyl-2-(2'-hydroxyphenyl)-benzimidazoles 2, 2-(2'-hydroxy-4'-alkoxyphenyl)-benzimidazoles 3, 2-(2',4'-dialkoxyphenyl)-benzimidazoles 4 and 1-alkyl-2-(2'-hydroxy-5'-nitrophenyl)-benzimidazoles 7 are synthesized by condensation of 2-hydroxybenzoic acid derivatives and o-phenylendiamine or its derivatives.Alkyl chains (C4, C8 or C12) are introduced by alkylation before or after the ring closure in order to increase the solubility of the reagent in toluene or n-octane.Furthermore the extraction properties of the benzimidazoles are investigated.Also some new analogous compounds of the benzothiazole and the 1,3,4-oxadiazole series were synthesized.