24454-82-8

Basic information

• Product Name: 2 3-DIETHOXYBENZALDEHYDE 97
• Synonyms: 2 3-DIETHOXYBENZALDEHYDE 97;2,3-Diethoxybenzaldehyde 97%
• CAS NO: 24454-82-8
• Molecular Formula: C₁₁H₁₄O₃
• Molecular Weight: 194.229
• Product Categories: Aldehydes;C10 to C21;Carbonyl Compounds
• Mol File: 24454-82-8.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 95-96 °C0.4 mm Hg(lit.)
• Flash Point: >230 °F
• Appearance: /
• Density: 1.070 g/mL at 25 °C(lit.)
• Vapor Pressure: 0.001mmHg at 25°C
• Refractive Index: n20/D 1.5200(lit.)
• CAS DataBase Reference: 2 3-DIETHOXYBENZALDEHYDE 97(CAS DataBase Reference)
• NIST Chemistry Reference: 2 3-DIETHOXYBENZALDEHYDE 97(24454-82-8)
• EPA Substance Registry System: 2 3-DIETHOXYBENZALDEHYDE 97(24454-82-8)

Safety Data

• Safety Statements: 24/25
• WGK Germany: 3
• Hazardous Substances Data: 24454-82-8(Hazardous Substances Data)

Usage

Structure

A benzene ring with two ethoxy groups and an aldehyde functional group

Type

Aldehyde derivative

Uses

Synthesis of pharmaceuticals, dyes, and perfumes; intermediate in organic synthesis; reagent in chemical reactions

Properties

Antibacterial and antifungal activities, potential use in antimicrobial agents development.

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

Upstream product

• 492-88-6 3-ethoxysalicylaldehyde 
• 75-03-6 ethyl iodide 
• 74-96-4 ethyl bromide 
• 24677-78-9 2,3-dihydroxybenzaldehyde 
• 64-67-5 diethyl sulfate 

Downstream Products

• 446051-40-7 methyl 3,4-diethoxydihydrocinnamate 
• 408353-03-7 2-(2,3-diethoxy-phenyl)ethylamine 
• 408353-28-6 1,2-diethoxy-3-(2-nitro-vinyl)benzene 
• 409109-85-9 2,3-diethoxy-benzoic acid-(2,3-diethoxy-phenethylamide) 
• 855648-06-5 5,6-diethoxy-1-(2,3-diethoxy-phenyl)-3,4-dihydro-isoquinoline 
• 861306-25-4 2,3-diethoxy-5-nitro-benzoic acid 
• 871880-26-1 2,3-diethoxy-5-nitro-benzaldehyde 
• 861302-91-2 2,3-diethoxy-5-bromo-benzaldehyde 
• 37860-70-1 2,3-diethoxy-benzoic acid 
• 861779-74-0 2,3-diethoxy-benzyl alcohol 

Relevant articles and documents

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.