181819-52-3

Basic information

• Product Name: 2 4-DIETHOXYBENZYL ALCOHOL
• Synonyms: 2,4-Diethoxybenzylalcohol
• CAS NO: 181819-52-3
• Molecular Formula: (C2H5O)2C6H3CH2OH
• Molecular Weight: 196.24
• Product Categories: Alcohols;C9 to C30;Oxygen Compounds
• Mol File: 181819-52-3.mol
• Article Data: 1

Chemical Properties

• Melting Point: 64-68 °C(lit.)
• Appearance: /
• Refractive Index: 1.512
• CAS DataBase Reference: 2 4-DIETHOXYBENZYL ALCOHOL(CAS DataBase Reference)
• NIST Chemistry Reference: 2 4-DIETHOXYBENZYL ALCOHOL(181819-52-3)
• EPA Substance Registry System: 2 4-DIETHOXYBENZYL ALCOHOL(181819-52-3)

Safety Data

• Hazard Codes: Xi
• Statements: 36
• Safety Statements: 26
• WGK Germany: 3
• Hazardous Substances Data: 181819-52-3(Hazardous Substances Data)

Usage

Physical state

White solid substance

Usage

Fragrance and flavor industry (scent ingredient), building block in the synthesis of various organic compounds, flavoring agent in food products (particularly confectionery and bakery items)

Odor

Pleasant, sweet, floral

Potential applications

Pharmaceutical industry (precursor for the synthesis of various drugs and pharmaceutical compounds)

InChI:InChI=1/C11H16O3/c1-3-13-10-6-5-9(8-12)11(7-10)14-4-2/h5-7,12H,3-4,8H2,1-2H3

Upstream product

• 95-01-2 2,4-Dihydroxybenzaldehyde 
• 22924-16-9 2,4-diethoxy-benzaldehyde 

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.