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

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

Uses

Used in Food Industry:
2-Furfurylpyridine is used as a flavoring agent for its smoky, nutty, and slightly spicy aroma, enhancing the taste profiles of various food products.
Used in Pharmaceutical Research:
2-Furfurylpyridine is studied for its potential anti-inflammatory and anti-cancer properties, making it a candidate for development in pharmaceutical applications aimed at treating inflammation and cancer-related conditions.
Used in Toxicology Studies:
Due to its presence in tobacco smoke and identified as a potential toxicant, 2-furfurylpyridine is utilized in toxicology research to understand its effects on human health and to develop strategies for mitigating its harmful impacts.

Upstream product

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

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.).

Versatile C(sp2)?C(sp3) Ligand Couplings of Sulfoxides for the Enantioselective Synthesis of Diarylalkanes

The reaction of chiral (hetero)aryl benzyl sulfoxides with Grignard reagents affords enantiomerically pure diarylalkanes in up to 98 % yield and greater than 99.5 % enantiomeric excess. This ligand coupling reaction is tolerant to multiple substitution patterns and provides access to diverse areas of chemical space in three operationally simple steps from commercially available reagents. This strategy provides orthogonal access to electron-deficient heteroaromatic compounds, which are traditionally synthesized by transition metal catalyzed cross-couplings, and circumvents common issues associated with proto-demetalation and β-hydride elimination.

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.