58860-84-7

Upstream product

• 98-88-4 benzoyl chloride 
• 79-37-8 oxalyl dichloride 
• 28547-23-1 4-(benzoyloxy)benzoic acid 
• 99-96-7 4-hydroxy-benzoic acid 

Downstream Products

• 85800-06-2 Phenyl-4(4-benzoyloxy)benzoyloxybenzoate 
• 1621377-93-2 4-benzoyloxy-N-(4-(trifluoromethyl)phenyl)benzamide 
• 1621377-79-4 1,3-bis(4-(benzoyloxy)phenyl)-1,2-dihydrobenzo[1,2,4]triazin-2-yl 
• 1621378-03-7 4-benzoyloxy-N-phenylbenzimidoyl chloride 
• 1621377-96-5 4-benzoyloxy-N-(4-(trifluoromethyl)phenyl)benzimidoyl chloride 
• 1621377-91-0 N'-(4-(benzoyloxy)phenyl)-N-phenyl-4-(benzoyloxy)benzenecarbohydrazonamide 
• 1621377-83-0 N'-(4-(benzoyloxy)phenyl)-N-[4-(trifluoromethyl)phenyl]-4-(benzoyloxy)benzenecarbohydrazonamide 
• 1621378-13-9 C₂₀H₁₃F₃N₃O₂ 
• 1621377-69-2 7-(trifluoromethyl)-1-(4-(benzoyloxy)phenyl)-3-(4-(benzyloxy)phenyl)-1,2-dihydrobenzo[1,2,4]triazin-2-yl 
• 300726-73-2 4-benzoyloxybenzanilide 
• 1621377-95-4 4-(benzoyloxy)-N-(4-iodophenyl)benzamide 
• 569-92-6 rhamnocitrin 
• 124458-87-3 2-(4-acetoxy-phenyl)-3,5,7-trimethoxy-chromen-4-one 
• 16692-52-7 3,4',5,7-tetramethoxyflavone 

Relevant academic research and scientific papers

2,2'-Binaphthalene Ester Chiral Dopants for Cholesteric Liquid Crystal Displays

A liquid crystal composition comprising a chiral dopant compound represented by the following structure (Structure 1): wherein: R1 and R2 are independently hydrogen, —(C═O)R9, —(C═O)R10, alkyl, aryl, alkaryl, alkenyl, cycloalkyl, alkoxyaryl, or heterocyclic all either substituted or unsubstituted, or combine to form a carbocyclic or heterocyclic ring; and R3-R9 are as described in the disclosure. Also featured are liquid crystal compositions comprising a chiral dopant compound represented by any of Structure 2-4 as described in the disclosure.

Functional group transformations in derivatives of 1,4-dihydrobenzo[1,2,4] triazinyl radical

Transformations of functional groups OCOPh, OCH2Ph, I, NO 2, and CO2Me in Blatter's radical derivatives 1-5 were investigated in order to develop synthetic tools for incorporation of the benzo[1,2,4]triazinyl system into c

Tetraoxybiphenyl Ester Chiral Dopants for Cholesteric Liquid Crystal Displays

A liquid crystal composition comprising a chiral dopant compound represented by the following formula: wherein: R1, R2 are independently aryl, alkyl, alkenyl, cycloalkyl, alkoxyaryl, alkaryl or heterocyclic all either substituted or unsubstituted, or combine to form a carbocyclic or heterocyclic ring; R3 and R4 are independently hydrogen, halogen, cyano, alkoxy, NHCOR7, NHSO2R7, COOR7, OCOR7, aryl, alkyl, alkenyl, cycloalkyl, alkoxyaryl, alkaryl or heterocyclic all either substituted or unsubstituted, or combine with either R1 or R2 to form a carbocylic or heterocyclic ring; R5 and R6 are independently hydrogen, CH2, CH, alkyl or aryl either substituted or unsubstituted, COOR7, or combine with L to form a carbocyclic or heterocyclic ring; R7 is aryl, alkyl, alkenyl, cycloalkyl, alkoxyaryl or heterocyclic all either substituted or unsubstituted; L is the non-metallic elements required to form a carbocyclic or heterocyclic ring, or a single bond or a double bond; m is 1-3; n is 0-12.

CHIRAL 3,4-DIHYDRO-2H-PYRAN COMPOUNDS

The invention relates to chiral 3,4-dihydro-2H-pyran compounds, to diastereomers thereof, and to the use of these compounds as chiral dopants for liquid crystal systems. The invention also relates to non-polymerizable or polymerizable liquid crystal compo

Liquid crystal compounds and intermediates thereof

A liquid crystal compound of the formula: STR1 wherein m and n are independently integers of 1 to 22; k and l are independently integers of 1 to 2; and C* is an asymmetric carbon atom, is chemically stable and can be applied to liquid crystal display devices operable at room temperature.

Synthesis and Thermal Transitions of Some Liquid Crystalline Oligomers

Fourteen aromatic ester oligomers have been synthesised, the majority of which have not been described previously.They can be considered as model compounds for liquid crystalline polyesters, and as such give useful information regarding the relationship between chemical structure and thermal properties.Such oligomers are also potentially important as precursors to liquid crystalline monomers.

GLUCOSIDES AND GLUCOSE ESTERS OF HYDROXYBENZOIC ACIDS IN PLANTS

Pinaceae; Brassicaceae; Solanaceae; Lamiaceae; hydroxybenzoic acid glucosides; hydroxybenzoylglucoses; glucose derivatives.Six hydroxybenzoic acid glucosides and three hydroxybenzoylglucoses were synthesized as reference substances and their content in plant extracts was determined by means of capillary GC and HPLC.The results suggest a wide distribution for the glucosides, whereas the glucose esters occur less frequently.

PHASE EQUILIBRIA IN LIQUID CRYSTALLINE SYSTEMS. PART I. SYNTHESIS AND LIQUID CRYSTALLINE PROPERTIES OF OLIGOMERS OF THE p-OXYBENZOATE SERIES.

Syntheses of the trimer (n equals 3), tetramer (n equals 4) and the pentamer (n equals 5) of the p-oxybenzoate series C//6H//5CO( minus OC//6H//4CO)//n// minus //2 minus OC//6H//5 are reported. Densities and thermal expansion coefficients of the neat liqu