5848-56-6

Basic information

• Product Name: (3-ethoxypropyl)benzene
• Synonyms: (3-ethoxypropyl)benzene;3-Phenylpropylethyl ether;Ethyl 3-phenylpropyl ether;Ethyl(3-phenylpropyl) ether;Ethylhydrocinnamyl ether;Einecs 227-441-3
• CAS NO: 5848-56-6
• Molecular Formula: C₁₁H₁₆O
• Molecular Weight: 164.24414
• EINECS: 227-441-3
• Mol File: 5848-56-6.mol
• Article Data: 15

Chemical Properties

• Boiling Point: 231.7°Cat760mmHg
• Flash Point: 94.8°C
• Appearance: /
• Density: 0.922g/cm³
• Vapor Pressure: 0.000603mmHg at 25°C
• Refractive Index: 1.512
• CAS DataBase Reference: (3-ethoxypropyl)benzene(CAS DataBase Reference)
• NIST Chemistry Reference: (3-ethoxypropyl)benzene(5848-56-6)
• EPA Substance Registry System: (3-ethoxypropyl)benzene(5848-56-6)

Safety Data

• Hazardous Substances Data: 5848-56-6(Hazardous Substances Data)

Usage

Description

(3-ethoxypropyl)benzene, also known by its IUPAC name 1-(3-ethoxypropyl)benzene, is a chemical compound that consists of a benzene ring with a 3-ethoxypropyl group attached to it. It has a chemical formula of C11H16O and a molecular weight of 164.24 g/mol. (3-ethoxypropyl)benzene has a faint sweet odor and is soluble in organic solvents such as ethanol, acetone, and benzene.

Uses

Used in Chemical Industry:
(3-ethoxypropyl)benzene is used as a solvent for various chemical reactions due to its solubility in organic solvents. It provides a suitable medium for the reactions to occur, facilitating the process and improving the yield of the desired products.
Used in Pharmaceutical Industry:
(3-ethoxypropyl)benzene is used as a chemical intermediate in the production of other organic compounds, including pharmaceuticals. Its unique structure allows it to be a building block for the synthesis of various drug molecules, contributing to the development of new medications.
Used in Research and Development:
(3-ethoxypropyl)benzene is utilized in research and development settings to study its properties and potential applications. Scientists and researchers explore its reactivity, stability, and interactions with other compounds to gain insights into its behavior and possible uses in various fields.

InChI:InChI=1/C13H14O4/c1-4-5-11-6-7-12(16-9(2)14)13(8-11)17-10(3)15/h4,6-8H,1,5H2,2-3H3

Upstream product

• 108-86-1 bromobenzene 
• 36865-40-4 1-bromo-3-ethoxypropane 
• 104-52-9 phenylpropyl chloride 
• 7148-78-9 3,3-diethoxyl-1-phenylprop-1-ene 
• 104-55-2 3-phenyl-propenal 
• 94-02-0 ethyl 3-oxo-3-phenylpropionate 
• 3277-26-7 1,1,3,3-Tetramethyldisiloxane 
• 2021-28-5 ethyl dihydrocinnamate 
• 16537-10-3 tert-butyl 3-phenylpropanoate 
• 617-86-7 triethylsilane 
• 122-97-4 3-Phenyl-1-propanol 
• 1569262-64-1 ethyl N-tert-butyl-4-nitrobenzenesulfonimidate 
• 122-72-5 3-phenylpropyl acetate 
• 111-35-3 3-ethoxy-1-propanol 

Downstream Products

• 4119-41-9 1-iodo-3-phenylpropan 
• 91345-74-3 ethyl-(3-bromo-3-phenyl-propyl)-ether 
• 143007-99-2 1-ethoxy-3-(morpholin-4-yl)-3-phenylpropane 
• 1294006-06-6 3-(4-fluorophenyl)propyl ethyl ether 
• 117694-89-0 4-ethoxypropylphenol 

Relevant articles and documents

Catalytic reductive deoxygenation of esters to ethers driven by hydrosilane activation through non-covalent interactions with a fluorinated borate salt

We report the catalytic and transition metal-free reductive deoxygenation of esters to ethers through the use of a hydrosilane and a fluorinated borate BArF salt as a catalyst. Experimental and theoretical studies support the role of noncovalent interactions between the fluorinated catalyst, the hydrosilane and the ester substrate in the reaction mechanism.

A Versatile Iridium(III) Metallacycle Catalyst for the Effective Hydrosilylation of Carbonyl and Carboxylic Acid Derivatives

A versatile iridium(III) metallacycle catalysed rapidly and selectively the reduction of a large array of challenging esters and carboxylic acids as well as various ketones and aldehydes. The reactions proceeded in high yields at room temperature by hydrosilylation followed by desilylation. Although the reactions of various aldehydes and ketones resulted exclusively in alcohols, the hydrosilylation of esters led to alcohols or ethers, depending on the type of substrate. Regarding the carboxylic acids, again the nature of the reagent controlled the outcome of the hydrosilylation reaction, either alcohols or aldehydes being formed.

Synthesis of ethers from esters via Fe-catalyzed hydrosilylation

Triiron dodecacarbonyl allows for the selective reduction of esters into the corresponding ethers. This protocol has a wide substrate scope. In addition, cholesteryl pelarogonate has been reduced under the reaction conditions with an excellent yield.