47225-92-3

Upstream product

• 96-49-1 [1,3]-dioxolan-2-one 
• 611-99-4 4,4'-Dihydroxybenzophenone 
• 540-51-2 2-bromoethanol 
• 75-21-8 oxirane 

Downstream Products

• 1417745-40-4 ((carbonylbis(4,4′-phenylene))bis(oxy))bis(ethane-2,1-diyl)bis(4-ethylbenzenesulfonate) 

Relevant academic research and scientific papers

Reactive mesogen and liquid crystal composition including the same

Provided are a reactive mesogen that may improve display quality of a liquid crystal display, and a liquid crystal composition including the same. The reactive mesogen is represented by the following Formula: where A1, A2, and A3 are each independently a substituted or unsubstituted divalent hydrocarbon ring, or a substituted or unsubstituted divalent heterocycle, L1 and L2 are each independently a direct linkage, —O—, —S—, —CO—, —COO—, —OCOO—, —O(CH2)k1—, —S(CH2)k1—, —O(CF2)k1—, —S(CF2)k1—, —(CH2)k1—, —CF2CH2—, —(CF2)k1—, —CH═CH—, —CF═CF—, —C≡C—, —CH═CH—COO—, or —(CH2)k1—COO—(CH2)k2—O—, Z1 and Z2 are each independently a direct linkage, —O—, —S—, —CO—, —COO—, —OCOO—, —O(CH2)m1—, —S(CH2)m1—, —O(CF2)m1—, —S(CF2)m1—, —(CH2)m1—, —CF2CH2—, —(CF2)m1—, —CH═CH—, —CF═CF—, —C≡C—, —CH═CH—COO—, —(CH2)m1—COO—, —(CH2)m1—COO—(CH2)m2—O—, —CH—(Sp—Pa)—, —CH2CH—(Sp—Pa)—, or —(CH—(Sp—Pa)—CH—(Sp—Pa))—, Pa is a polymerizable group, B is an unsubstituted heterocycle, a substituted or unsubstituted crown ether group, or wherein T1 and T2 are each independently —OH, —CH3, —CF3, —CHF2, —CH2F, —CH2Br, —CHBr2, —CHCl2, or —CH2Cl.

New bis-thiazolium analogues as potential antimalarial agents: Design, synthesis, and biological evaluation

Bis-thiazolium salts are able to inhibit phosphatidylcholine biosynthesis in Plasmodium and to block parasite proliferation in the low nanomolar range. However, due to their physicochemical properties (i.e., permanent cationic charges, the flexibility, and lipophilic character of the alkyl chain), the oral bioavailability of these compounds is low. New series of bis-thiazolium-based drugs have been designed to overcome this drawback. They feature linker rigidification via the introduction of aromatic rings and/or a decrease in the overall lipophilicity through the introduction of heteroatoms. On the basis of the structure-activity relationships, a few of the promising compounds (9, 10, and 11) were found to exhibit potent antimalarial in vitro and in vivo activities (EC50 50 ip 0.7 mg/kg).

Material for photo-alignment layer, photo-alignment layer and method of manufacturing the same

The present invention provides a photo-alignment layer for a liquid crystal display device, which has good liquid crystal display device characteristics such as a good voltage holding ratio and also has good alignment stability and sufficient resistance t