102408-54-8

Upstream product

• 767-00-0 4-cyanophenol 
• 118591-51-8 2-(methoxymethylene)dodecanal 
• 38148-63-9 p-amidinophenol hydrochloride 

Downstream Products

• 129832-80-0 (S)-2-Fluoro-hexanoic acid 4-(5-decyl-pyrimidin-2-yl)-phenyl ester 
• 129851-63-4 (S)-2-Fluoro-heptanoic acid 4-(5-decyl-pyrimidin-2-yl)-phenyl ester 
• 118406-54-5 (+)-5-Decyl-2-pyrimidine 
• 129832-81-1 (S)-2-Fluoro-nonanoic acid 4-(5-decyl-pyrimidin-2-yl)-phenyl ester 
• 118406-57-8 (S)-2-Fluoro-decanoic acid 4-(5-decyl-pyrimidin-2-yl)-phenyl ester 
• 460359-37-9 5-Decyl-2-(4-{8-[dimethyl-(2-trimethylsilanyl-ethyl)-silanyl]-octyloxy}-phenyl)-pyrimidine 
• 127981-51-5 2-bromo-4-(5-decyl-2-pyrimidinyl)phenol 
• 122300-25-8 p-(5-n-decyl-2-pyrimidyl)phenyl 2-cyano-2-methylhexanoate 
• 153580-92-8 2-{4-[(8-bromooctyl)oxy]phenyl}-5-decylpyrimidine 
• 1403575-03-0 2-[4-(4-bromobutoxy)phenyl]-5-decylpyrimidine 
• 1403575-41-6 1-{8-[4-(5-decylpyrimidin-2-yl)phenoxy]octyl}-3-[4-(dodecyloxy)phenyl]imidazolium bromide 
• 1403575-35-8 1-{4-[4-(5-decylpyrimidin-2-yl)phenoxy]butyl}-3-[4-(dodecyloxy)phenyl]imidazolium bromide 
• 1403575-32-5 3-dodecyl-1-{8-[4-(5-decylpyrimidin-2-yl)phenoxy]octyl}imidazolium bromide 
• 1403575-29-0 3-dodecyl-1-{4-[4-(5-decylpyrimidin-2-yl)phenoxy]butyl}imidazolium bromide 

Relevant academic research and scientific papers

Towards room temperature ionic liquid crystals: Linear versus bent imidazolium phenylpyrimidines

The synthesis and the mesomorphic properties of novel imidazolium salts with mesogenic 2-phenylpyrimidine or 2-alkylpyrimidinecarboxylic acid central cores are reported. The mesogenic units are connected to the imidazolium head groups via an alkoxy spacer

Optically active compound, liquid crystal composition containing the same, and liquid crystal electro-optic element using the same

An optically active compound represented by formula (I): wherein A represents wherein R2 represents an alkyl group having from 8 to 12 carbon atoms; R1 represents a straight chain alkyl group having from 2 to 5 carbon atoms; X represents a fluorine atom or a methyl group; n represents 1 or 2; m represents an integer of from 0 to 3; and C* represents an asymmetric carbon atom, and a liquid crystal composition containing the same are disclosed. The compound exhibits large spontaneous polarization and low viscosity and, when added to an achiral base liquid crystal composition, induces a chiral nematic phase in which the helical pitch has small temperature dependence.