58573-94-7

Usage

Uses

Used in Liquid Crystal Synthesis:
4-(4'-N-HEPTYLPHENYL)BENZOIC ACID is used as an intermediate in the synthesis of liquid crystals for its unique properties that contribute to the formation of stable liquid crystal structures.
Used in Organic Electronics:
4-(4'-N-HEPTYLPHENYL)BENZOIC ACID has potential applications in the field of organic electronics due to its chemical properties that can be harnessed in the development of electronic devices and components.
Used in Chemical and Industrial Processes:
The heptyl substitution on the phenyl group of 4-(4'-N-HEPTYLPHENYL)BENZOIC ACID provides it with unique properties that make it useful in a variety of chemical and industrial processes, enhancing the performance of products and processes in these industries.

Upstream product

• 67599-21-7 4'-n-Heptyl-biphenyl-4-carbonsaeureamid 
• 41122-71-8 4-heptyl-4'-cyanobiphenyl 

Downstream Products

• 61733-20-8 4-(4-n-heptylphenyl)-benzoic acid 4'-ethylphenyl ester 
• 61733-21-9 4-(4-n-heptylphenyl)-benzoic acid 4'-n-propylphenyl ester 
• 61733-38-8 4'-Heptyl-biphenyl-4-carboxylic acid 4-propoxy-phenyl ester 
• 61733-22-0 4-(4-n-heptylphenyl)-benzoic acid 4'-n-butylphenyl ester 
• 1392007-35-0 4-(4-N-heptylphenyl)benzoic acid 4-cyano-3,5-difluorophenyl ester 
• 124513-32-2 [16-(4'-Heptyl-biphenyl-4-carbonyl)-1,4,10,13-tetraoxa-7,16-diaza-cyclooctadec-7-yl]-(4'-heptyl-biphenyl-4-yl)-methanone 
• 124513-34-4 7,16-Bis-(4'-heptyl-biphenyl-4-ylmethyl)-1,4,10,13-tetraoxa-7,16-diaza-cyclooctadecane 
• 126257-60-1 4''-(n-Heptyl)biphenyl-4'-carbonsaeure-cyclohexylester 
• 58573-87-8 4'-heptylbiphenyl-4-ylcarboxylic acid chloride 
• 61733-36-6 4'-Heptyl-biphenyl-4-carboxylic acid 4-methoxy-phenyl ester 

Relevant academic research and scientific papers

COMPOUNDS WITH ACTIVITY AT RETINOIC ACID RECEPTORS

Disclosed herein are novel compounds with activity at RARβ 2 receptors. Further disclosed are the use of such compounds for treatment of or to alleviate symptoms of cancer, neurological disorders such as memory deficits and schizophrenia, neurodegenerative disorders such as Parkinson's and Alzheimer's diseases, inflammatory disorders such as psoriasis and rheumatoid arthritis, eye disorders and depression.

Liquid crystal compound

A liquid crystal compound represented by the following general formula: wherein R* stands for an alkyl group having an asymmetric carbon atom, R stands for a linear alkyl group, and A stands for STR1

LIQUID CRYSTAL ORIENTATION ON VARIOUS SURFACES.

The liquid crystal orientation on various surfaces were investigated by using the ″Liquid Crystal Chromatography,″ which is useful for observing the true orientation by eliminating impurities in the liquid crystal materials. As the result, it was found that all nematic liquid crystals of Schiff base-, biphenyl-, ester-, PCH-, and azoxy-compounds aligned parallel to the surfaces of In//2O//3, Al//2O//3, soda-lime glass, SiO, etc. On the other hand, some of these liquid crystals such as MBBA, 5CB have been known to have a tendency to align perpendicular to the surface like In//2O//3. Then, the reason of this discrepancy was also investigated and it was found that impurities produced by hydrolysis of these liquid crystals had amphiphilic characteristic which induced a perpendicular alignment of these liquid crystals.

Biphenyl esters and liquid crystalline mixtures comprising them

Biphenyl esters of the formula STR1 wherein X is --CO--O-- or --O--CO-- and R1 and R2 each are alkyl or alkoxy of 1 - 8 carbon atoms, enlarge significantly the temperature range of the nematic phase of liquid-crystalline compositions without adversely affecting other properties.