10496-51-2

Basic information

• Product Name: 2-(2-furfurylidene)cyclohexan-1-one
• Synonyms: 2-(2-Furfurylidene)cyclohexan-1-one; AI3-05663; Cyclohexanone, 2-(2-furanylmethylene)-; 2-(furan-2-ylmethylidene)cyclohexanone
• CAS NO: 10496-51-2
• Molecular Formula: C₁₁H₁₂O₂
• Molecular Weight: 176.2118
• EINECS: 234-025-5
• Mol File: 10496-51-2.mol
• Article Data: 13

Chemical Properties

• Boiling Point: 301.2°C at 760 mmHg
• Flash Point: 137.5°C
• Density: 1.147g/cm³
• Vapor Pressure: 0.00107mmHg at 25°C
• Refractive Index: 1.575
• CAS DataBase Reference: 2-(2-furfurylidene)cyclohexan-1-one(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(2-furfurylidene)cyclohexan-1-one(10496-51-2)
• EPA Substance Registry System: 2-(2-furfurylidene)cyclohexan-1-one(10496-51-2)

Safety Data

• Hazardous Substances Data: 10496-51-2(Hazardous Substances Data)

Usage

Structure

Cyclic ketone with a furan ring and a cyclohexane ring

Usage

Starting material or building block in organic synthesis and pharmaceutical research, production of fragrances and flavoring agents

Biological activities

Potential antitumor and anti-inflammatory properties

Industry applications

Chemical and pharmaceutical industries

Medicinal properties

Attraction for potential therapeutic uses

Upstream product

• 98-01-1 furfural 
• 108-94-1 cyclohexanone 

Downstream Products

• 351498-01-6 2-furfurylidenecyclohexan-1-one thiosemicarbazone 
• 102026-78-8 2-((Ξ)-furfurylidene)-cyclohexanone-(2,4-dinitro-phenylhydrazone) 
• 95164-74-2 optically inactive 2-((Ξ)-furfurylidene)-6-[[2]furyl-(2-oxo-cyclohexyl)-methyl]-cyclohexanone 
• 85123-22-4 4-furan-2-yl-3-phenyl-1-oxa-2-aza-spiro[4.5]dec-2-en-6-one 
• 3208-11-5 2-(5-Hydroxy-pentyl)-cyclohexanol 
• 171617-11-1 α-furyl-methyl-cyclohexanone 
• 67823-66-9 2-furfuryl-cyclohexylamine 
• 18134-29-7 (2-Furan-2-ylmethyl-cyclohexyl)-methyl-amine 

Relevant articles and documents

Enolization and Aldol reactions of ketone with a La3+-immobilized organic solid in water. A microporous enolase mimic [4]

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Redox-Neutral Cobalt(III)-Catalyzed C-H Activation/Annulation of α,β-Unsaturated Oxime Ether with Alkyne: One-Step Access to Multisubstituted Pyridine

A redox neutral Co(III)-catalyzed annulation of α,β-unsaturated oxime ether with alkyne has been reported. Multisubstituted pyridines were synthesized in good yields without the use of any heavy metal oxidants. The developed methodology tolerates a variety of functional groups. Notably, this transformation has been applied to the late-stage modification of the bioactive molecule dehydropregnenolone.

Fe3O4 nanoparticles as an efficient and magnetically recoverable catalyst for the synthesis of α β-unsaturated heterocyclic and cyclic ketones under solvent-free conditions

An efficient and green procedure has been developed for the synthesis of monoarylidenes of cyclic and heterocyclic ketones. The reaction was carried out under solvent-free conditions in the presence of a catalytic amount of nanosized magnetite (Fe3O4). The catalyst was easily removed by using an external magnet. The structures of the products were deduced from their 1H NMR, 13C NMR, and infrared spectroscopy and mass spectrometry. [Supplementary materials are available for this article. Go to the publisher's online edition of Synthetic Communications for the following free supplemental resource(s): Full experimental and spectral details.]