135310-65-5

Upstream product

• 109-06-8 α-picoline 
• 623-27-8 terephthalaldehyde, 

Downstream Products

• 106366-65-8 methyl α-cyano-4-<2-(2-pyridyl)ethenyl>cinnamate 
• 53031-52-0 (E)-4-(2-(pyridin-2-yl)vinyl)benzoic acid 
• 135413-76-2 1,3-Dicyano-2,4-bis-(4-{3-cyano-3-methoxycarbonyl-2-pyridin-2-yl-4-[4-((E)-2-pyridin-2-yl-vinyl)-phenyl]-cyclobutyl}-phenyl)-cyclobutane-1,3-dicarboxylic acid dimethyl ester 
• 135413-75-1 1-Cyano-3-[4-((E)-2-cyano-2-ethoxycarbonyl-vinyl)-phenyl]-2-pyridin-2-yl-4-[4-((E)-2-pyridin-2-yl-vinyl)-phenyl]-cyclobutanecarboxylic acid ethyl ester 
• 135413-74-0 methyl 1-cyano-3-<4-(2-cyano-2-methoxycarbonylethenyl)phenyl>-2-(2-pyridyl)-4-<4-<2-(2-pyridyl)ethenyl>phenyl>cyclobutanecarboxylate 
• 135413-77-3 C₇₆H₆₄N₈O₈ 
• 124067-51-2 ethyl α-cyano-4-<2-(2-pyridyl)ethenyl>cinnamate 

Relevant academic research and scientific papers

Synthesis, optical, and thermal properties of conjugated, bispyridyl and tetrapyridyl compounds by Knoevenagel reaction

A series of conjugated, bispyridyl and tetrapyridyl compounds were synthesized from either terephthalaldehyde or isophthalaldehyde and activated pyridyl compounds by Knoevenagel reaction on heating in acetic anhydride in presence of acetic acid and their

One- and two-photon-induced isomerization of styryl compounds possessing A-π-A′ structure

Two styryl compounds with A-π-A′ structure that feature a fixed pyridine ring as an electron acceptor (A) and pyridine or 5,6,7,8-tetrahydroisoquinoline cation as the other acceptor (A′) have been synthesized. Their structures were elucidated by means of

X-ray structures of precursors of styrylpyridine-derivatives used to obtain 4-((E)-2-(pyridin-2-yl)vinyl)benzamido-TEMPO: Synthesis and characterization

The synthesis and characterization of the precursor isomers trans-4-(2-(pyridin-2-yl)vinylbenzaldehyde (I), trans-4-(2-(pyridin-4-yl)vinylbenzaldehyde (II), trans-4-(2-(pyridin-2-yl)vinylbenzoic acid (III) and (E)-4-(2-(pydridin-4-yl)vinylbenzoic acid (IV