123370-63-8

Upstream product

• 123-11-5 4-methoxy-benzaldehyde 
• 431-03-8 dimethylglyoxal 
• 124268-87-7 {(E)-2-(4-methoxyphenyl)ethenyl}magnesium bromide 
• 59417-06-0 1,4-dimethyl-2,3-dioxopiperazine 

Downstream Products

• 1174046-03-7 6,6'-bis(1H-indol-3-yl)-4,4'-di-4-methoxyphenyl-2,2'-bipyridinyl-5,5'-dicarbonitrile 
• 1198427-61-0 7,7,7',7'-tetramethyl-4,4'-bis(4-methoxyphenyl)-4,6,7,8,4',6',7',8'-octahydro-1H,1H-[2,2']biquinolinyl-5,5'-dione 
• 5422-12-8 2,3‐bis((E)?4‐methoxystyryl)quinoxaline 
• 1257421-72-9 5,6-bis[(E)-2-(4-methoxyphenyl)vinyl]-3-pyrazin-2-yl-1,2,4-triazine 
• 1257421-67-2 5,6-bis[(E)-2-(4-methoxyphenyl)vinyl]-3-pyridin-4-yl-1,2,4-triazine 
• 1257421-61-6 5,6-bis[(E)-2-(4-methoxyphenyl)vinyl]-3-pyridin-2-yl-1,2,4-triazine 
• 1255524-60-7 (5RS,6SR)-5,6-bis(4-methoxyphenyl)cycloheptane-1,3-dione 

Relevant academic research and scientific papers

First hyperpolarizabilities of hexaazatriphenylene derivatives: Octupolar nonlinear optical molecules

The first evaluation of the β values and thermal stability for octupolar molecules derived from hexaazatriphenylene derivatives is reported.

An anticancer-active imidazole analogue as a fluorescent sensor: sensitive and selective detection of Cu2+ ions

A highly sensitive and selective imidazole-based fluorescent “on–off” probe, (2-(4,5-bis((E)-4-methoxystyryl)-1H-imidazol-2-yl) phenol) (BMIP), is synthesized and characterized. The fluorescence of the compound is quenched by Cu2+ ions, contrar

NOVEL SMALL MOLECULES THAT BIND AND/OR MODULATE DIFFERENTFORMS OF TAU OLIGOMERS

The present invention relates to novel small molecules of Formulas I, II, III, Ilia, Illb, and IV and pharmaceutically acceptable salts thereof, as well as the preparation and the use thereof.

Preparation of cycloheptane ring by nucleophilic cyclopropanation of 1,2-diketones with bis(iodozincio)methane

The nucleophilic cyclopropanation of hexa-1,5-diene-3,4-diones with bis(iodozincio)methane afforded the Zn alkoxides of cis-dialkenylcyclopropane-1,2-diols stereoselectively. The subsequent oxy-Cope rearrangement afforded the corresponding Zn alkoxides of

N-heterocyclic carbene catalyzed reaction of cinnamils leading to the formation of 2,3,8-triaryl vinyl fulvenes: An uncommon transformation

An unexpected transformation of 1,6-diarylhexa-1,5-diene-3,4-diones (cinnamils) to 2,3,8-triaryl vinyl fulvenes via N-Heterocyclic Carbene (NHC) catalysis is reported. Mechanistic as well as synthetic novelty is the hallmark of this reaction.