93109-27-4

Upstream product

• 17754-90-4 4-(Diethylamino)salicylaldehyde 
• 100-39-0 benzyl bromide 

Downstream Products

• 1268353-64-5 C₄₀H₄₂N₆O₂ 
• 1378233-64-7 2-(2-(benzyloxy)-4-(diethylamino)benzylidene)malononitrile 
• 1435269-32-1 C₃₁H₃₇NO₅ 
• 1435269-41-2 C₃₁H₃₇NO₅ 
• 1435269-51-4 C₃₁H₃₅NO₅ 
• 1435269-63-8 C₃₁H₃₅NO₅ 
• 1435269-72-9 C₂₄H₃₁NO₅ 
• 1435269-79-6 C₂₄H₃₁NO₅ 
• 17754-90-4 4-(Diethylamino)salicylaldehyde 

Relevant academic research and scientific papers

Rapid detection of aspartic acid and glutamic acid in water by BODIPY-Based fluorescent probe: Live-cell imaging and DFT studies

Strategically modified4-(diethylamino)-2-(pyridin-2-ylmethoxy)benzaldehyde appended BODIPY-based probe N,N-SP-BPY detects aspartic acid (Asp)and glutamic acid (Glu)by inhibition of Photoinduced electron transfer (PET)process in water. The probe shows cons

Aggregation-induced emission enhancement materials with large red shifts and their self-assembled crystal microstructures

Two simple intramolecular charge transfer compounds (BzBMN and BzFAN), derived from 2-benzyloxy-4-diethylaminobenzaldehyde, have been synthesized. Unlike typical AIEE molecules, the enhanced emission of these compounds in the solid state is accompanied by large red shifts in emission wavelength. Absorption and photoluminescence (PL) spectra of the compounds in solution, film and the X-ray single crystal structures were investigated to understand the mechanism of enhanced emission in the solid state. The results indicate that the bathochromic shift excimer-like emissions originated from dimers induced by the dipole-dipole interaction and long-range ordered arrangement (e.g. J-aggregation), and the enhanced emission is attributed to the restriction of intramolecular rotations caused by multiple intermolecular hydrogen bonding interactions. In addition, it was also observed that BzBMN and BzFAN can facilely form single crystal microbelts and microtubes by a simple reprecipitation method. The Royal Society of Chemistry 2011.

Effect of phenyl ring substitution on J-aggregate formation ability of novel bisazomethine dyes in vapour-deposited films

Bisazomethine dyes, which are synthesized using diaminomaleonitrile and aminobenzaldehydes, exhibit red fluorescence in solution and in the solid state. Several bisazomethine dyes are known to form J-aggregates in vapour-deposited films. In this work, novel bisazomethine dyes were synthesized and the effect of phenyl ring substitution on the J-aggregate formation in vapour-deposited films was examined. The optical properties of the dyes were examined in solution and in the solid state through molecular orbital calculations. Four derivatives were found to form J-aggregates in vapour-deposited films as determined from the shape of the spectrum and the absorption edge.

NOVEL CURCUMIN DERIVATIVE

The present invention provides a novel compound that is structurally similar to curcumin and has a suppressive effect on Aβ aggregation, a degradative effect on Aβ aggregates, an inhibitory effect on β-secretase, and a protective effect on neurons. The novel compound is a compound represented by the following general formula (Ia) or a salt thereof: wherein R1 represents a 4-hydroxy-3-methoxyphenyl group or the like, and R2 represents a 1H-indol-6-yl group or the like.