85666-05-3

Usage

Uses

Used in Pharmaceutical Industry:
(E)-4-(2-(pyridin-3-yl)vinyl)phenol is used as a potential therapeutic agent for the treatment of cancer and inflammation. Its antioxidant and anti-inflammatory properties make it a promising candidate for the development of pharmaceutical drugs targeting these conditions.
Used in Materials Science:
(E)-4-(2-(pyridin-3-yl)vinyl)phenol is used as a component in the development of organic electronic devices. Its unique molecular structure and electronic properties contribute to its potential application in this field, where it may be utilized to enhance the performance of such devices.

Upstream product

• 501-81-5 pyridyl-3-yl-acetic acid 
• 123-08-0 4-hydroxy-benzaldehyde 
• 5863-78-5 (E)-3-(4-methoxystyryl)pyridine 
• 824-94-2 p-methoxybenzyl chloride 
• 99-96-7 4-hydroxy-benzoic acid 
• 1120-90-7 3-iodopyridine 
• 7400-08-0 p-Coumaric Acid 
• 105-13-5 4-Methoxybenzyl alcohol 
• 121-98-2 methyl 4-methoxybenzoate 
• 1145-93-3 diethyl 4-methoxybenzylphosphonate 

Downstream Products

• 879009-51-5 ethyl [4-[(E)-2-pyridin-3-ylvinyl]phenoxy]acetate 

Relevant academic research and scientific papers

Tandem heck/decarboxylation/heck strategy: Protecting-group-free synthesis of symmetric and unsymmetric hydroxylated stilbenoids

Ride the (micro)wave: The title strategy has been developed for the synthesis of various symmetric or unsymmetric hydroxylated stilbenoids utilizing 4-halophenols and acrylic acid as coupling partners (see scheme; DMA=N,N-dimethylacetamide, MW=microwave). Protecting groups are not necessary and a single palladium catalyst is used. Copyright

Synthesis and anti-inflammatory activity of resveratrol analogs

Seventeen novel resveratrol derivatives were synthesized. Their anti-inflammatory activities were tested on xylene-induced mouse ear edema. The pharmacological results showed that some compounds have potent anti-inflammatory activities.

Antiinflammatory 2,6-Di-tert-butyl-4-(2-arylethenyl)phenols

A series of 2,6-di-tert-butyl-4-(2-arylethenyl)phenols was prepared and examined for their ability to inhibit cyclooxygenase and 5-lipoxygenase in vitro and developing adjuvant arthritis in vivo in the rat.Structure-activity relationships are discussed.Am

Pyridyl-substituted-benzofurans

The present invention provides novel pyridinyl-benzofurans and derivatives thereof which are useful as thromboxane A2 (TXA2) synthetase inhibitors and as such represent potent pharmacological agents.