6075-11-2

Basic information

• Product Name: 1,5-Di(2-furanyl)-3-pentanone
• Synonyms: 1,5-Di(2-furanyl)-3-pentanone
• CAS NO: 6075-11-2
• Molecular Formula: C₁₃H₁₄O₃
• Molecular Weight: 218.25
• EINECS: 228-011-8
• Mol File: 6075-11-2.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 309.3°C at 760 mmHg
• Flash Point: 142°C
• Appearance: /
• Density: 1.118g/cm³
• Vapor Pressure: 0.000643mmHg at 25°C
• Refractive Index: 1.514
• CAS DataBase Reference: 1,5-Di(2-furanyl)-3-pentanone(CAS DataBase Reference)
• NIST Chemistry Reference: 1,5-Di(2-furanyl)-3-pentanone(6075-11-2)
• EPA Substance Registry System: 1,5-Di(2-furanyl)-3-pentanone(6075-11-2)

Safety Data

• Hazardous Substances Data: 6075-11-2(Hazardous Substances Data)

Usage

General Description

1,5-Di(2-furanyl)-3-pentanone is a chemical compound with the molecular formula C13H14O2. It is also known as 5,5'-Bis(2-furyl)-2,2-dimethyl-3-pentanone and is a ketone derivative with two furanyl rings attached to a pentanone backbone. 1,5-Di(2-furanyl)-3-pentanone is commonly used as a flavoring agent in the food industry due to its pleasant aroma and taste, resembling that of caramel and vanilla. It is also used as a fragrance ingredient in perfumes and cosmetics. Additionally, 1,5-Di(2-furanyl)-3-pentanone has potential applications in pharmaceuticals and medicinal chemistry due to its unique chemical structure. However, it is important to handle this compound with care as it may pose health risks if not properly managed.

InChI:InChI=1/C13H14O3/c14-11(5-7-12-3-1-9-15-12)6-8-13-4-2-10-16-13/h1-4,9-10H,5-8H2

Upstream product

• 886-77-1 (E,E)-1,5-di-(2-furyl)pent-1,4-dien-3-one 
• 886-77-1 1,5-bis-(2-furanyl)-1,4-pentandien-3-one 
• 98-01-1 furfural 
• 64-17-5 ethanol 
• 74-88-4 methyl iodide 
• 144850-49-7 difurfurylideneacetone 

Downstream Products

• 6265-26-5 1,5-di(2-tetrahydrofuryl)-3-pentanol 
• 5451-23-0 9-tetrahydro[2]furyl-nonane-1,4,7-triol 
• 5467-13-0 tridecane-1,4,7,10,13-pentaol 

Relevant articles and documents

Synthesis of Renewable Lubricant Alkanes from Biomass-Derived Platform Chemicals

The catalytic synthesis of liquid alkanes from renewable biomass has received tremendous attention in recent years. However, bio-based platform chemicals have not to date been exploited for the synthesis of highly branched lubricant alkanes, which are currently produced by hydrocracking and hydroisomerization of long-chain n-paraffins. A selective catalytic synthetic route has been developed for the production of highly branched C23 alkanes as lubricant base oil components from biomass-derived furfural and acetone through a sequential four-step process, including aldol condensation of furfural with acetone to produce a C13 double adduct, selective hydrogenation of the adduct to a C13 ketone, followed by a second condensation of the C13 ketone with furfural to generate a C23 aldol adduct, and finally hydrodeoxygenation to give highly branched C23 alkanes in 50.6 % overall yield from furfural. This work opens a general strategy for the synthesis of high-quality lubricant alkanes from renewable biomass.

INFLUENCE OF HYDROGEN PRESSURE ON THE RATE AND MECHANISM OF HYDROGENATION OF DIFURFURYLIDENEACETONE IN PRESENCE OF SKELETAL NICKEL-TITANIUM-ALUMINUM CATALYST

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