1073142-73-0

Basic information

• Product Name: 1-(chloromethyl)-3,5-diethoxybenzene
• Synonyms: 1-(chloromethyl)-3,5-diethoxybenzene
• CAS NO: 1073142-73-0
• Molecular Formula: C₁₁H₁₅ClO₂
• Molecular Weight: 214.6886
• Mol File: 1073142-73-0.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 311.5±27.0 °C(Predicted)
• Appearance: /
• Density: 1.083±0.06 g/cm3(Predicted)
• CAS DataBase Reference: 1-(chloromethyl)-3,5-diethoxybenzene(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(chloromethyl)-3,5-diethoxybenzene(1073142-73-0)
• EPA Substance Registry System: 1-(chloromethyl)-3,5-diethoxybenzene(1073142-73-0)

Safety Data

• Hazardous Substances Data: 1073142-73-0(Hazardous Substances Data)

Upstream product

• 26153-38-8 3,5-dihydroxybenzaldehyde 
• 120355-79-5 3,5-diethoxybenzaldehyde 
• 198623-56-2 3,5-diethoxybenzyl alcohol 

Downstream Products

• 1073142-68-3 C₂₄H₂₃NO₃ 

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.