116223-55-3

Upstream product

• 110-53-2 1-Bromopentane 
• 540-38-5 p-Iodophenol 
• 39905-50-5 4-pentyloxyaniline 

Downstream Products

• 158938-08-0 4′′-(pentyloxy)-1,1′:4′,1′′-terphenyl-4-carboxylic acid 
• 1562687-86-8 1,4-bis[4(n-pentyloxy)phenyl]butane 
• 1352545-34-6 1-(3,4,5-trimethoxyphenyl)-5-(4-(pentyloxy)phenyl)-1H-tetrazole 
• 34296-23-6 1,2-bis(4-n-pentyloxyphenyl)acetylene 
• 79887-16-4 1-ethynyl-4-(pentyloxy)benzene 
• 170784-80-2 2-(4-pentyloxyphenyl)-1,3-propanediol 
• 29148-21-8 diethyl (4-pentyloxyphenyl)malonate 
• 540492-15-7 1-(4-n-pentyloxyphenyl)-2-trimethylsilylacetylene 
• 125151-55-5 4-(p-pentyloxyphenyl)-2-methyl-3-butyn-2-ol 

Relevant academic research and scientific papers

Ordering of apolar and polar solutes in nematic solvents

To illustrate the relative importance of electrostatic interactions, the LC-NMR data for a pair of polar and apolar solutes that are structural isomers, ortho- and para-dichlorobenzene, respectively, dissolved in polar and apolar nematogens were analyzed.

Highly ordered smectic structures of disc-rod luminescent liquid crystals: The role of the tolane group

Two novel calamitic tolane luminogen-modified triphenylene-based discotic luminescent liquid-crystals (LLC) were rationally designed and synthesized to investigate the self-assembly competition between triphenylene discogens and tolane calamitic mesogens.

Synthesis of some novel aromatic alkynyl silanes: Mesomorphic characterization of ethynyl-substituted rod-shaped molecules

The synthesis and characterization of 10 new rod-shaped substituted benzoates possessing the 4-(2-trimethylsilyl)ethynyl group in terminal phenyl position is reported employing the simple and efficient Sonogashira cross-coupling and DCC esterification. 4′

Synthesis of diphenyl-diacetylene-based nematic liquid crystals and their high birefringence properties

We synthesized two series of diphenyl-diacetylene (DPDA)-based materials with alkoxy and alkyl tails of length m (DPDA-OCm and DPDA-Cm, respectively), and measured their nematic-phase birefringence (Δn) as a function of wavelength and temperature. We found that Δn decreases with an increase in m, possibly by a dilution effect of the low-Δn alkyl tail. Further, of the two series, Δn was found to be relatively higher in the DPDA-OCm materials, with the highest value of 0.4 obtained for DPDA-OC1 at 550 nm at 10 °C below the isotropic-to-nematic transition temperature. Further, we observed the temperature dependence for Δn, which is proportional to the order parameter (s). From extrapolation to s = 1 (the perfect orientation state), it is speculated that the DPDA-O moiety has the potential to afford a very large Δn of 0.9. The Royal Society of Chemistry 2012.

NOVEL HETEROCYCLIC AMIDE DERIVATIVES HAVING DIHYDROOROTATE DEHYDROGENASE INHIBITING ACTIVITY

Novel heterocyclic amide derivatives having pharmacological effects, that is, compounds represented by the general formula (1) or salts thereof: (1) wherein X1-X2 is S-CH2 or the like; R1 is alkyl or the like; p is 0 to 7; R2 is hydrogen, alkyl, or the like; R3 is hydrogen, alkyl, or the like; Y1-Y2 is CH=CH or the like; R4 is halogeno, alkyl, or the like; q is 0 to 4; and R5 is halogeno, hydrogen, alkyl, or the like.

Synthesis and mesomorphic properties of some fluorinated benzoate liquid crystals

Three series of [4-(4′-n-alkyloxyphenyl)acetylenyl]-2,6- difluorophenyl fluorinated benezoates and one series of fluorinated benzoates with 2,3,5,6-tetrafluorophenylene group and semi-perfluorocarbon chain have been synthesized. Their phase transition temperatures have been measured by texture observation in a polarizing microscope and confirmed by DSC. For the series without fluorocarbon chains, increasing the quantity of fluorosubstituents on the terminal phenyl groups decreased nematic stability (TN-I), but the breadth of the SmA phase range was increased. Lateral fluorosubstitution in the central group lowered the nematic stability (TN-I) and decreased the breadth of the SmA phase range. The series with semiperfluorocarbon chains were more likely to form SmA phases than the series with hydrogencarbon chains, and with the increasing of fluorosubstituents quantity on the terminal phenyl groups nematic and SmA stability (TN-I and TsmA-N) were both decreased.

Solid dimorphism of tetra-arylcyclobutadienecobalt derivatives bearing long aliphatic lateral groups

A new series of disk-like cyclobutadienecobalt derivatives symmetrically substituted by lateral alkoxy groups with different chain lengths (-O(CH2)nCH3, n=5, 6, 8, and 12) were prepared and their thermal phase transition b

Synthesis and mesomorphic properties of some fluoro-substituted benzoates

Several series of fluoro-substituted benzoate liquid crystals have been synthesized. The results showed that the SmA phase is enhanced with the increasing of the degree of fluoro-substitution on the para- and meta-position of the terminal phenyl groups. And the molecules which have same molecular structural formula show nearly the same melting points. It is also discussed about the effect of the ester bond's direction on the mesomorphic properties.