5032-11-1

Basic information

• Product Name: bis(4-ethoxyphenyl)methanone
• CAS NO: 5032-11-1
• Molecular Formula: C₁₇H₁₈O₃
• Molecular Weight: 270.323
• Mol File: 5032-11-1.mol
• Article Data: 9

Chemical Properties

• Boiling Point: 415.6°C at 760 mmHg
• Flash Point: 196.8°C
• Density: 1.087g/cm³
• Vapor Pressure: 4.09E-07mmHg at 25°C
• Refractive Index: 1.545
• CAS DataBase Reference: bis(4-ethoxyphenyl)methanone(CAS DataBase Reference)
• NIST Chemistry Reference: bis(4-ethoxyphenyl)methanone(5032-11-1)
• EPA Substance Registry System: bis(4-ethoxyphenyl)methanone(5032-11-1)

Safety Data

• Hazardous Substances Data: 5032-11-1(Hazardous Substances Data)

Upstream product

• 7322-75-0 4,4'-diethoxythiobenzophenone 
• 74-96-4 ethyl bromide 
• 611-99-4 4,4'-Dihydroxybenzophenone 
• 5031-92-5 1,1-Bis(4-ethoxyphenyl)ethylene 
• 64-19-7 acetic acid 
• 75-03-6 ethyl iodide 
• 108-88-3 toluene 
• 554-70-1 triethylphosphine 
• 62897-87-4 2,2-bis-(4-ethoxy-phenyl)-1,1,1-tribromo-ethane 
• 119072-55-8 tert-butylisonitrile 
• 22237-13-4 (4-ethoxyphenyl)boronic acid 
• 588-96-5 4-bromoethoxybenzene 
• 541-41-3 chloroformic acid ethyl ester 
• 201230-82-2 carbon monoxide 

Downstream Products

• 93727-67-4 4,4'-diethoxy-benzhydrol 
• 610-54-8 2,4-dinitro-1-ethoxybenzene 
• 56920-81-1 4,4'-(prop-1-ene-1,1-diyl)bis(ethoxybenzene) 
• 88534-40-1 9-[bis(4-methoxyphenyl)methylidene]-9H-fluorene 
• 1105506-23-7 3-iodo-4,4'-diethoxybenzophenone 
• 36374-73-9 C₂₀H₂₆O₄ 
• 5031-96-9 2.2-Bis-(4'-ethoxyphenyl)acetaldehyd 
• 60883-74-1 1-bromo-2,2-bis(p-ethoxyphenyl)-1-phenylethene 
• 735271-53-1 1,1-bis-(4-ethoxy-phenyl)-2-phenyl-ethene 
• 102171-98-2 3,3-bis-(4-ethoxy-phenyl)-acrylic acid 
• 2132-71-0 2,2-Dichloro-1,1-bis(4-ethoxyphenyl)ethylene 
• 54655-90-2 1,1,4,4-tetrakis-(4-ethoxy-phenyl)-buta-1,3-diene 
• 2132-65-2 1,1-bis-(4-ethoxy-phenyl)-2-bromo-ethene 
• 2132-67-4 1,1-bis-(4-ethoxy-phenyl)-2-chloro-ethene 

Relevant articles and documents

Regioselective Diboron-Mediated Semireduction of Terminal Allenes

A method for the regioselective reduction of the terminal double bond of 1,1-disubstituted allenes has been developed. In the presence of a palladium catalyst, tetrahydroxydiboron and stoichiometric water, allene semireduction proceeds in high yield to afford Z-alkenes selectively.

Palladium/Copper-Catalyzed Oxidative Coupling of Arylboronic Acids with Isocyanides: Selective Routes to Amides and Diaryl Ketones

An efficient and alternative oxidative cross-coupling strategy starting from arylboronic acids and isocyanides for the selective synthesis of amides and diaryl ketones with palladium/copper catalysis is developed. Various substituted benzamides and benzop

Pd/Cu-cocatalyzed aerobic oxidative carbonylative homocoupling of arylboronic acids and CO: A highly selective approach to diaryl ketones

A highly selective Pd/Cu-cocatalyzed aerobic oxidative carbonylative homocoupling of arylboronic acids has been developed. This method employs a simple catalytic system, readily available boronic acids as the substrates, molecular oxygen as the oxidant, and 1 atm of CO/O2, which makes this method practical for further applications.