61657-61-2

Usage

Uses

Used in Pharmaceutical Synthesis:
4-DIETHYLAMINO-2-ETHOXY-BENZALDEHYDE is utilized as a key intermediate in the synthesis of various pharmaceuticals and organic compounds. Its unique structure contributes to the development of new drugs with specific therapeutic properties.
Used as a Flavoring Agent:
In the food and beverage industry, 4-DIETHYLAMINO-2-ETHOXY-BENZALDEHYDE serves as a flavoring agent, enhancing the taste profiles of different products. Its distinct aromatic properties make it a valuable ingredient in creating unique flavor experiences.
Used in Fragrance Production:
4-DIETHYLAMINO-2-ETHOXY-BENZALDEHYDE is also employed in the production of fragrances, where its strong odor plays a crucial role in creating long-lasting and complex scent profiles for various applications, including perfumes, cosmetics, and household products.
Used in Chemical Research:
In the field of chemical research, 4-DIETHYLAMINO-2-ETHOXY-BENZALDEHYDE is used as a reagent and a building block for the synthesis of novel compounds with potential applications in various industries, including materials science and medicinal chemistry.

InChI:InChI=1/C13H19NO2/c1-4-14(5-2)12-8-7-11(10-15)13(9-12)16-6-3/h7-10H,4-6H2,1-3H3

Upstream product

• 17754-90-4 4-(Diethylamino)salicylaldehyde 
• 74-96-4 ethyl bromide 

Downstream Products

• 1268353-61-2 C₃₀H₃₈N₆O₂ 
• 73268-86-7 3-(2-ethoxy-4-diethylamino-phenyl)-2-cyano-acrylic acid ethyl ester 

Relevant academic research and scientific papers

Synthesis of novel colorants for DSSC to study effect of alkyl chain length alteration of auxiliary donor on light to current conversion efficiency

Five (MA1-MA5) hemicyanine based sensitizer having N, N-diethyl aniline as a primary donor and hydroxy or alkoxy as an auxiliary donor have been synthesized to establish a correlation between amphiphilic nature of the sensitizer and charge recombination. A strong electron withdrawing 3-(carboxymethyl)-2-methylbenzo[d]thiazol-3-ium bromide has been explored as an acceptor. All the dyes were characterized by 1H-NMR, 13C-NMR and CHN analysis. The photophysical properties of these dyes were recorded in seven different solvents which do not show any significant impact on absorption and emission maxima while molar absorptivity coefficient decreases with increase in alkyl chain length. These dyes show very poor emission in all the solvents. Nano-crystalline mesoporous TiO2 based dye-sensitized solar cells were fabricated using MA1 to MA5 sensitizers to evaluate their photovoltaic performance. MA5 having six carbon alkyl chain shows maximum efficiency of 4.97% while MA1 without any alkyl chain shows the lowest efficiency of 3.40%. As the length of alkyl chain increase efficiency increase due to increment in short circuit current (Jsc) and retardation in the recombination process. Density functional theory (DFT) and time-dependent density functional theory (TD-DFT) were explored to obtain vertical excitation, HOMO-LUMO energy and electron density distribution.

Emergence through delicate balance between the steric factor and molecular orientation: a highly bright and photostable DNA marker for real-time monitoring of cell growth dynamics

Due to its remarkable structural and optical stability in biological milieu, a newly developed small molecule based DNA marker with high brightness (Φ = 0.51, brightness = 26?300 M?1 cm?1) and almost zero toxicity has been explored. For the first time to our knowledge, this approach has provided real-time monitoring of growth and reproductive potency of living cells beyond nine days.

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.