17920-86-4

Basic information

• Product Name: Di-furan-2-yl-methanone
• Synonyms: Di-furan-2-yl-methanone
• CAS NO: 17920-86-4
• Molecular Formula: C₉H₆O₃
• Molecular Weight: 162.14214
• Mol File: 17920-86-4.mol
• Article Data: 10

Chemical Properties

• Appearance: /
• Storage Temp.: Inert atmosphere,Room Temperature
• CAS DataBase Reference: Di-furan-2-yl-methanone(CAS DataBase Reference)
• NIST Chemistry Reference: Di-furan-2-yl-methanone(17920-86-4)
• EPA Substance Registry System: Di-furan-2-yl-methanone(17920-86-4)

Safety Data

• Hazardous Substances Data: 17920-86-4(Hazardous Substances Data)

Usage

General Description

Di-furan-2-yl-methanone, also known as difuryl ketone, is a chemical compound with a molecular formula C10H8O2. It is a yellow crystalline solid and is commonly used as a building block in the synthesis of various organic compounds. Di-furan-2-yl-methanone is widely used in the pharmaceutical and agrochemical industries for the production of drugs, pesticides, and other chemical products. It is also used as a flavoring agent in the food and beverage industry. Additionally, this compound has potential applications in materials science and organic electronics due to its unique electronic and optical properties. However, caution should be taken when handling di-furan-2-yl-methanone as it may have hazardous effects if not properly managed.

Upstream product

• 527-69-5 2-furancarbonyl chloride 
• 37104-40-8 2,2'-(hydroxymethylene)difuran 
• 123209-18-7 N-aniline 
• 617-90-3 2-furancarbonitrile 
• 110-00-9 furan 
• 79-44-7 N,N-Dimethylcarbamoyl chloride 
• 201230-82-2 carbon monoxide 
• 687-48-9 ethyl N,N-dimethylcarbamate 
• 32315-10-9 bis(trichloromethyl) carbonate 
• 123209-11-0 N-aniline 
• 492-94-4 furil 
• 13331-23-2 fur-2-ylboronic acid 

Downstream Products

• 1197-40-6 2,2'-difurylmethane 
• 2689-59-0 (furan-2-yl)(phenyl)methanone 

Relevant articles and documents

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.

Ytterbium triflate catalyzed Friedel-Crafts reaction: Facile synthesis of diaryl ketones

Friedel-Crafts reaction of aromatic compounds (benzenes, thiophene, furan, pyrrole, naphthalene, and benzothiophene) with bis(trichloromethyl) carbonate [BTC] was efficiently catalyzed by ytterbium triflate [Yb(OTf)3] to give diaryl ketones wit

Palladium-catalyzed carbonylative coupling of organolead compounds: Synthesis of symmetrical ketones

Organolead acetates can be carbonylated in the presence of Pd2(dba)3·CHCl3 (5mol%) and NaOMe (5 equiv.) in CH3CN under atmospheric pressure of carbon monoxide at room temperature to afford symmetrical ketones.