74421-02-6

Basic information

• Product Name: 2-Decylpyridine
• Synonyms: 2-Decylpyridine
• CAS NO: 74421-02-6
• Molecular Formula: C15H25N
• Molecular Weight: 219.3657
• Mol File: 74421-02-6.mol
• Article Data: 7

Chemical Properties

• Boiling Point: 289.9 °C at 760 mmHg
• Flash Point: 147.3 °C
• Appearance: /
• Density: 0.886 g/cm³
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 2-Decylpyridine(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Decylpyridine(74421-02-6)
• EPA Substance Registry System: 2-Decylpyridine(74421-02-6)

Safety Data

• Hazardous Substances Data: 74421-02-6(Hazardous Substances Data)

Usage

General Description

2-Decylpyridine is a chemical compound with the molecular formula C15H25N. It is an organic compound that belongs to the class of pyridine derivatives. 2-Decylpyridine is commonly used as a flavoring agent in the food industry due to its strong, nutty flavor. It is also used in the production of pharmaceuticals and other organic chemicals. 2-Decylpyridine can be toxic if ingested in large quantities and should be handled with care. It is a clear, colorless liquid at room temperature and is soluble in organic solvents. This chemical has a variety of industrial and commercial applications, making it a versatile and valuable compound in the chemical industry.

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Relevant articles and documents

PHOSPHINE FREE COBALT BASED CATALYST, PROCESS FOR PREPARATION AND USE THEREOF

The present invention discloses a phosphine free cobalt based catalyst of formula (I) and a process for preparation thereof. The present invention further discloses a process for the synthesis of aromatic heterocyclic compounds of formula (II) and pyrazine derivative using the phosphine free cobalt based catalyst of formula (I).

Practical routes to 2,6-disubstituted pyridine derivatives

We report the synthesis of a series of 2,6-disubstituted pyridines in a straightforward manner starting from readily available 2-substituted pyridines. The main sequence involves a selective ?-lithiation reaction with halogen functionalization followed by

Iron-catalyzed chemoselective cross-coupling of primary and secondary alkyl halides with arylzinc reagents

Functional-group-compatible cross-coupling reaction of alkyl halides with arylzinc reagents takes place under iron catalysis in the presence of TMEDA, producing a variety of aromatic compounds in good to excellent yield. The pronounced effect of a magnesium salt was found to be the key to the promotion of the iron-catalyzed coupling reaction. Georg Thieme Verlag Stuttgart.