4912-58-7

Basic information

• Product Name: 3-ETHOXY-4-HYDROXYBENZYL ALCOHOL
• Synonyms: RARECHEM AL BD 0103;3-ETHOXY-4-HYDROXYBENZYL ALCOHOL
• CAS NO: 4912-58-7
• Molecular Formula: C₉H₁₂O₃
• Molecular Weight: 168.19
• Product Categories: Benzhydrols, Benzyl & Special Alcohols
• Mol File: 4912-58-7.mol

Chemical Properties

• Melting Point: 73-75°C
• Boiling Point: 323.3 °C at 760 mmHg
• Flash Point: 149.3 °C
• Appearance: /
• Density: 1.182 g/cm³
• Vapor Pressure: 0.000109mmHg at 25°C
• Refractive Index: 1.558
• CAS DataBase Reference: 3-ETHOXY-4-HYDROXYBENZYL ALCOHOL(CAS DataBase Reference)
• NIST Chemistry Reference: 3-ETHOXY-4-HYDROXYBENZYL ALCOHOL(4912-58-7)
• EPA Substance Registry System: 3-ETHOXY-4-HYDROXYBENZYL ALCOHOL(4912-58-7)

Safety Data

• Hazardous Substances Data: 4912-58-7(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Industry:
3-Ethoxy-4-hydroxybenzyl alcohol is used as an intermediate in the synthesis of various pharmaceutical compounds, contributing to the development of new drugs and therapeutic agents.
Used in Organic Chemistry:
As a building block in organic chemistry, 3-Ethoxy-4-hydroxybenzyl alcohol is utilized in the creation of complex organic molecules and the advancement of chemical research.
Used in Antioxidant Applications:
Identified as a potential antioxidant, 3-Ethoxy-4-hydroxybenzyl alcohol is employed for its ability to combat oxidative stress, which can be beneficial in various health and medical applications.
Used in Biological Research:
3-Ethoxy-4-hydroxybenzyl alcohol's unique structure and properties make it a valuable tool in biological research, aiding in the study of various biological processes and mechanisms.

InChI:InChI=1/C9H12O3/c1-2-12-9-5-7(6-10)3-4-8(9)11/h3-5,10-11H,2,6H2,1H3

Upstream product

• 121-32-4 4-hydroxy-3-ethoxybenzaldehyde 
• 64-17-5 ethanol 

Downstream Products

• 78826-07-0 (+/-)-2-(2-ethoxy-4-hydroxymethylphenoxy)propionic acid 
• 1000378-07-3 8-methylnonanoic acid (3-ethoxy-4-hydroxyphenyl)methyl ester 
• 70959-77-2 5-{2-[2-(2-Ethoxy-4-hydroxymethyl-phenoxy)-ethylamino]-1-hydroxy-ethyl}-2-methoxy-benzenesulfonamide 
• 70958-89-3 5-{1-Hydroxy-2-[2-(2-ethoxy-4-hydroxymethylphenoxy)ethylamino]ethyl}-2-methylbenzenesulfonamide 
• 70958-73-5 [4-(2-Benzylamino-ethoxy)-3-ethoxy-phenyl]-methanol 
• 96840-56-1 2-ethoxy-4-isopropoxymethylphenol 
• 71119-07-8 2-ethoxy-4-ethoxymethylphenol 
• 5595-79-9 2-ethoxy-4-(methoxymethyl)phenol 

Relevant articles and documents

Phosphoric acid-modified commercial kieselguhr supported palladium nanoparticles as efficient catalysts for low-temperature hydrodeoxygenation of lignin derivatives in water

Efficient production of high value-added chemicals and biofuels via low-temperature chemoselective HDO of lignin derivatives in water is still a challenge. Here, we construct a low-cost, active and stable Pd/PCE catalyst using phosphoric acid-modified commercial Celite (PCE) as the support, and this catalyst exhibits excellent activity in low-temperature HDO of vanillin as well as other lignin derivatives in water. The superior catalytic performance is due to the presence of P species on the surface of Pd/PCE, accelerating the selective conversion of the intermediate into the final product. Detailed experimental and mechanistic studies reveal that the rapid conversion of the intermediate to the final product proceeds via a free-radical process in an interfacial microenvironment created by intimate interacting between the P species and Pd NPs. The insights of this work provide a new low-cost catalytic system for efficient production of valuable chemicals and future biofuels from lignin derivatives. This journal is

Self-Assembly and Host-Guest Interactions of Pd3L2Metallo-cryptophanes with Photoisomerizable Ligands

New photoswitchable pyridyl-azo-phenyl-decorated tripodal host ligands (Laz) that belong to the cyclotriveratrylene family have been synthesized, and their photoswitching behavior and crystal structures determined. The latter includes a remarkable 7-fold

Thioether type compound as well as synthesis method and application thereof

The invention provides a thioether type compound and also relates to a synthesis method of the thioether type compound and application of the thioether type compound. A chemical structure of the thioether type compound enables the thioether type compound to have a relatively high melting point and be not easily sublimated, so that the thioether type compound has relatively good thermal stability;the thioether type compound has an excellent anti-oxidization capability and has no toxic and side effects, so that the thioether type compound has relatively high utilization safety; secondly, a target compound is synthesized by the synthesis method of the thioether type compound, provided by the invention, by adopting one-step reaction; visibly, the synthesis method is simple to operate, moderate in technological conditions, green and environmentally friendly, and is very suitable for large-scale industrial production. A series of experiments prove that the thioether type compound has an obvious inhibition effect on oxidization of various foods and an anti-oxidization effect of the compound has a certain dose-effect relationship with the concentration of the compound; therefore, the thioether type compound provided by the invention has a wide application prospect and a good market potential.

Synthesis and Absolute Configuration of Chiral (C3) Cyclotriveratrylene Derivatives. Crystal Structure of (M)-(-)-2,7,12-Triethoxy-3,8,13-tris--10,15-dihydro-5H-tribenzocyclononene

The absolute configuration of chiral C3-cyclotriveratrylene derivatives has been determined unambiguously as follows.First, the absolute configuration of 2-(2-ethoxy-4-hydroxymethylphenoxy)propionic acid (5b) was established as R-(+) by chemica