22924-16-9

Usage

Uses

Used in Pharmaceutical and Fine Chemicals Synthesis:
2,4-DIETHOXY-BENZALDEHYDE is used as a key intermediate in the synthesis of various pharmaceuticals and fine chemicals for its ability to be readily incorporated into complex molecular structures, contributing to the development of new therapeutic agents and specialty compounds.
Used as a Flavoring Agent in the Food Industry:
In the food industry, 2,4-DIETHOXY-BENZALDEHYDE is used as a flavoring agent to impart its characteristic sweet and floral notes to a variety of food products, enhancing their sensory appeal.
Used in Medicinal Applications:
2,4-DIETHOXY-BENZALDEHYDE is used as a potential therapeutic agent for its pharmacological activities, such as anti-inflammatory and analgesic properties, which may contribute to the treatment of various conditions requiring pain relief and inflammation reduction.
Used in Research and Development:
In the scientific community, 2,4-DIETHOXY-BENZALDEHYDE is utilized in research and development for exploring its chemical properties and potential applications in new areas of chemistry and medicine, including the development of novel drug delivery systems or as a probe in biochemical studies.

InChI:InChI=1/C11H14O3/c1-3-13-10-6-5-9(8-12)11(7-10)14-4-2/h5-8H,3-4H2,1-2H3

Upstream product

• 74-90-8 hydrogen cyanide 
• 2049-73-2 2,4-diethoxybenzene 
• 75-03-6 ethyl iodide 
• 95-01-2 2,4-Dihydroxybenzaldehyde 
• 108-46-3 recorcinol 
• 1141669-81-9 1-(2,4-diethoxyphenyl)ethanol 
• 74-96-4 ethyl bromide 

Downstream Products

• 86726-46-7 2-(2,4-Diethoxy-benzylidene)-malonic acid diethyl ester 
• 84272-94-6 (4-Chloro-phenyl)-[1-(2,4-diethoxy-phenyl)-meth-(E)-ylidene]-amine 
• 86726-27-4 5-(2,4-Diethoxy-benzyl)-2-imino-thiazolidin-4-one 
• 86733-83-7 5-(2,4-Diethoxy-benzyl)-thiazolidine-2,4-dione 
• 86726-51-4 2-(2,4-Diethoxy-benzyl)-malonic acid diethyl ester 
• 86726-56-9 2-Chloro-2-(2,4-diethoxy-benzyl)-malonic acid diethyl ester 
• 181819-52-3 2,4-diethoxybenzyl alcohol 
• 223699-50-1 2,4-diethoxybenzonitrile 
• 19074-30-7 2,4-diethoxybenzoic acid 
• 5681-19-6 4-(2,4-diethoxy-benzylidene)-2-phenyl-4H-oxazol-5-one 
• 105337-91-5 (E)-2,4-diethoxy-β-nitro-styrene 

Relevant academic research and scientific papers

Use of o-hydroxy-p-methoxybenzaldehyde derivative as herbicide

The invention discloses an application of an o-hydroxy p-methoxybenzaldehyde derivative as a herbicide. The o-hydroxy-p-methoxybenzaldehyde derivative and the herbicide taking the o-hydroxy-p-methoxybenzaldehyde derivative as a component are used for preventing and removing weeds in a field crop growth place and a non-farming crop place.

In vitro study and structure-activity relationship analysis of stilbenoid derivatives as powerful vasorelaxants: Discovery of new lead compound

The development of vasorelaxant as the antihypertensive drug is important as it produces a rapid and direct relaxation effect on the blood vessel muscles. Resveratrol (RV), as the most widely studied stilbenoid and the lead compound, inducing the excellent vasorelaxation effect through the multiple signalling pathways. In this study, the in vitro vascular response of the synthesized trans-stilbenoid derivatives, SB 1-8e were primarily evaluated by employing the phenylephrine (PE)-precontracted endothelium-intact isolated aortic rings. Herein we report trans-3,4,4′-trihydroxystilbene (SB 8b) exhibited surprisingly more than 2-fold improvement to the maximal relaxation (Rmax) of RV. This article also highlights the characterization of the aromatic protons in terms of their unique splitting patterns in 1H NMR.

Stepwise degradation of hydroxyl compounds to aldehydes: Via successive C-C bond cleavage

Stepwise degradation of hydroxyl compounds to aldehydes via successive cleavage of C-C bonds was achieved by using a bimetallic catalytic system (PdCl2 + CuCl) without any ligands and additives. The broad applicability is expanded to a diverse range of aromatic, aliphatic, primary and secondary alcohols, as well as lignin model compounds.