30478-77-4

Basic information

• Product Name: 1-(furan-2-yl)pentan-1-ol
• CAS NO: 30478-77-4
• Molecular Formula: C₉H₁₄O₂
• Molecular Weight: 154.2063
• Mol File: 30478-77-4.mol
• Article Data: 13

Chemical Properties

• Boiling Point: 201°C at 760 mmHg
• Flash Point: 75.4°C
• Density: 1.009g/cm³
• Vapor Pressure: 0.193mmHg at 25°C
• Refractive Index: 1.481
• CAS DataBase Reference: 1-(furan-2-yl)pentan-1-ol(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(furan-2-yl)pentan-1-ol(30478-77-4)
• EPA Substance Registry System: 1-(furan-2-yl)pentan-1-ol(30478-77-4)

Safety Data

• Hazardous Substances Data: 30478-77-4(Hazardous Substances Data)

Usage

General Description

1-(furan-2-yl)pentan-1-ol is a chemical compound with the molecular formula C10H14O2. It is a colorless liquid with a furan ring attached to a pentanol chain. This chemical is commonly used as a flavoring agent and fragrance in the food and beverage industry due to its sweet, floral, and fruity aroma. It is also utilized in the synthesis of various pharmaceuticals and organic compounds. Additionally, 1-(furan-2-yl)pentan-1-ol has been studied for its potential antioxidant and antimicrobial properties, making it a compound of interest for various applications in the fields of medicine and healthcare.

Upstream product

• 98-01-1 furfural 
• 693-03-8 n-butyl magnesium bromide 
• 110-00-9 furan 
• 78508-98-2 lithium (2S,3R)-2,3-(N,O-benzylidyne)-2-amino-3-hydroxy-butyrate 
• 109-72-8 n-butyllithium 
• 109-65-9 1-bromo-butane 
• 103560-62-9 (2E)-4-oxo-2-nonenal 
• 614-99-3 Ethyl 2-furoate 
• 693-04-9 butyl magnesium bromide 

Downstream Products

• 37174-92-8 4-oxo-nonanoic acid ethyl ester 
• 14032-66-7 5-hydroxy-2-(5H)-furanone 
• 110-62-3 pentanal 
• 3194-17-0 1-furan-2-yl-pentan-1-one 
• 623-93-8 5-nonanol 
• 13686-96-9 nonane-1,5-diol 
• 4940-17-4 2-butyl-3-hydroxy-4-pyrone 
• 16695-34-4 (E)-4-none-1-ol 
• 132381-19-2 2-(1-Phenylsulfanyl-pentyl)-tetrahydro-furan 
• 134340-65-1 N-(1-(furan-2-yl)pentyl)-4-methylbenzenesulfonamide 
• 99062-45-0 1-(furan-2-yl)pentan-1-amine 

Relevant articles and documents

Reaction products of γ-tocopherol with (E)-4-oxo-2-nonenal in acidic acetonitrile

γ-Tocopherol was reacted with (E)-4-oxo-2-nonenal (ONE) at 37 °C in an acidic acetonitrile solution. The reaction products were isolated by reversed-phase high-performance liquid chromatography and their structures were characterized to be 5-substituted γ

Photooxygenation of azidoalkyl furans: Catalyst-free triazole and new endoperoxide rearrangement

Photooxygenation of azidoalkyl furans has revealed both a novel triazole formation method and a unique endoperoxide rearrangement. The key step of this method is a 3 + 2 cycloaddion of the azide to the endoperoxide intermediate. The reduction of the peroxide bond and two subsequent C-C bond cleavages provide a triazole having a newly formed carboxylic acid functionality. The reactions are clean and efficient with yields ranging from 60% to 90%.

A novel one-pot synthesis of secondary alcohols from esters

Alkylation or vinylation by using organometallic reagents after partial reduction of carboxylic esters with LDBBA gave secondary alcohols, also involving allyl alcohols, without any isolation of intermediates in good yield (54-78%).