106584-05-8

Basic information

• Product Name: 2-FURFURYLPYRIDINE
• Synonyms: 2-FURFURYLPYRIDINE;2-(Furan-2-ylmethyl)pyridine
• CAS NO: 106584-05-8
• Molecular Formula: C10H9NO
• Molecular Weight: 159.18
• Mol File: 106584-05-8.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 2-FURFURYLPYRIDINE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-FURFURYLPYRIDINE(106584-05-8)
• EPA Substance Registry System: 2-FURFURYLPYRIDINE(106584-05-8)

Safety Data

• Hazardous Substances Data: 106584-05-8(Hazardous Substances Data)

Usage

General Description

2-Furfurylpyridine is a chemical compound that consists of a pyridine ring with a furfuryl group attached to it. It is often used as a flavoring agent in the food industry due to its smoky, nutty, and slightly spicy aroma. The compound is also found in tobacco smoke and has been identified as a potential toxicant in cigarette smoke. Additionally, 2-furfurylpyridine has been studied for its potential anti-inflammatory and anti-cancer properties, making it of interest in the field of pharmaceutical research. Overall, 2-furfurylpyridine is a versatile compound with potential applications in various industries.

Upstream product

• 584-12-3 2-bromofuran 
• 941279-81-8 2,4-dimethyl-3-(pyridin-2-ylmethyl)pentan-3-ol 
• 109-06-8 α-picoline 
• 856591-70-3 C₁₀H₉NOS 
• 98-02-2 2-thiolomethyl-furan 
• 109-09-1 2-chloropyridine 
• 106584-08-1 1-Methyl-2-(2-furylmethyl)pyridinium iodide 

Downstream Products

• 93560-49-7 furan-2-yl(pyridin-2-yl)methanone 

Relevant articles and documents

Efficient Selenium-Catalyzed Selective C(sp3)?H Oxidation of Benzylpyridines with Molecular Oxygen

An efficient selenium-catalyzed direct oxidation of benzylpyridines in aqueous DMSO has been successfully developed by using molecular oxygen as the oxidant. A variety of benzoylpyridines with broad functional group tolerance were obtained in modest to excellent yields and with exclusive chemoselectivity. (Figure presented.).

REARRANGEMENT OF 2-HETARYLALKYLPYRIDINIUM SALTS

The rearrangement of 2-thienyl- and 2-furylalkylpyridinium salts to the corresponding anilines by the action of methylammonium sulfites has been studied.It has been shown that the rearrangement of these salts is accompanied in many cases by the formation of phenols and dealkylation products.The influence of the length of the alkyl chain between the heterocyclic rings on the ratio of the rearrangement products has been investigated.