33905-63-4

Upstream product

• 36823-84-4 4-pentyloxybenzoyl chloride 
• 99-96-7 4-hydroxy-benzoic acid 
• 177715-63-8 4-pentyloxy-benzoic acid ethyl ester 
• 15872-41-0 4-(pentyloxy)benzoic acid 
• 110-53-2 1-Bromopentane 
• 71-41-0 pentan-1-ol 
• 120-47-8 Ethyl 4-hydroxybenzoate 
• 123-31-9 hydroquinone 
• 148731-04-8 4-Pentyloxy-benzoic acid 4-benzyloxy-phenyl ester 

Downstream Products

• 100201-93-2 5-Butyl-pyridine-2-carboxylic acid 4-(4-pentyloxy-benzoyloxy)-phenyl ester 
• 1427167-70-1 4-acryloyloxyphenyl 4-amyloxybenzoate 
• 1427167-73-4 4-(2,3-epoxypropoxy)phenyl 4-amyloxybenzoate 
• 33905-70-3 C₂₆H₂₆O₆ 

Relevant academic research and scientific papers

Mesogenic 4-acryloyloxy- and 4-(2,3-epoxypropoxy)phenyl 4-alkoxybenzoates

Procedures were developed which made it possible to synthesize in good yields homologs of 4-acryloyloxyphenyl 4-alkoxybenzoates (C3, C 5, C7, C8) and of 4-(2,3-epoxypropoxy)phenyl 4-alkoxybenzoates (C5, C7). The substituted phenylbenzoates obtained exhibit the enantiotropic nematic mesomorphism in a sufficiently wide temperature range. The studied compounds have absorption maxima in the near UV region and a high temperature of decomposition beginning.

Study of activation energy and order of reaction of some liquid crystals

Liquid crystals of the type p-phenylene-di-p-n-alkoxy benzoate have been prepared. Kissinger isothermal decomposition method has been used for determination of activation energy values of liquid crystals. Kissinger's assessment for shape index of DTA peaks is used to find the order of reaction. There is no direct relationship between the carbon atoms in terminal methylene groups and Ea values. Order of reaction value decreases with increase in heating rate upto carbon atoms 10 in the terminal methylene group but beyond this the order increases or decreases.

1,1'-Disubstituted Ferrocene-Containing Thermotropic Liquid Crystals of Structure 5-C5H4)COOC6H4XC6H4OCnH2n+1>2> (X=OOC or COO). Influence of the Orientation of the Central Ester Function on the Mesogenic Properties

The two series I and II of 1,1'-disubstituted ferrocenes which differ by the direction of the ester function included the rigid organic part were synthesized and their liquid crystal properties examined.These latter were found to be strongly dependent on the orientation of the connecting ester group and on the alkyl chain.