1122-69-6

Usage

Uses

Used in Pharmaceutical and Agrochemical Industries:
2-Ethyl-6-methylpyridine is utilized as a key intermediate in the synthesis of various pharmaceuticals and agrochemicals. Its unique chemical structure allows for the development of new compounds with specific therapeutic or pesticidal properties, enhancing the range of available treatments and crop protection options.
Used as a Flavoring Agent in the Food and Beverage Industry:
In the food and beverage sector, 2-Ethyl-6-methylpyridine is employed to impart distinctive flavors to a variety of products. Its strong odor and unique taste characteristics make it a valuable ingredient in the creation of complex flavor profiles, contributing to the sensory experience of consumers.
Safety and Handling:
Given its classification as a hazardous substance, 2-Ethyl-6-methylpyridine requires careful handling and storage to prevent exposure. Proper safety measures, including the use of personal protective equipment and adherence to storage guidelines, are crucial to minimize potential harm to human health and the environment.

InChI:InChI=1/C8H11N/c1-3-8-6-4-5-7(2)9-8/h4-6H,3H2,1-2H3

Upstream product

• 109-06-8 α-picoline 
• 3248-28-0 dipropionyl peroxide 
• 75-03-6 ethyl iodide 
• 802294-64-0 propionic acid 
• 108-48-5 2,6-dimethylpyridine 
• 74-88-4 methyl iodide 
• 1122-70-9 2-methyl-6-vinylpyridine 
• 19760-15-7 1-ethyl-2-methylpyridinium iodide 
• 64-17-5 ethanol 
• 7647-01-0 hydrogenchloride 
• 856834-88-3 2-(2-bromo-ethyl)-6-methyl-pyridine 
• 7664-41-7 ammonia 
• 934-78-1 2-(6-methylpyridin-2-yl)-ethanol 
• 18368-63-3 6-chloro-2-picoline 

Downstream Products

• 856857-19-7 (6-ethyl-[2]pyridyl)-acetic acid ethyl ester 
• 38275-04-6 octane-2,6-dione 
• 499-83-2 Pyridine-2,6-dicarboxylic acid 
• 935-28-4 2,6-diethylpyridine 

Relevant academic research and scientific papers

Silica-supported tripod triarylphosphane: Application to transition metal-catalyzed C(sp3)-H borylations

A silica-supported tripod triarylphosphane (Silica-3p-TPP), containing a triphenylphosphane-type core tripodally immobilized on the silica surface, allows rhodium- and iridium-catalyzed C(sp3)-H borylations of amide, urea and alkylpyridine derivatives. The 31P CP/MAS NMR studies for the coordination behavior of the tripod phosphane towards a rhodium complex indicate efficient site isolation of the each phosphane center, allowing independent mono-P-coordination to the metal center.

Polymerization initiator, modified-conjugated diene polymer and tire prepared therefrom

The present disclosure relates to a polymerization initiator and a modified conjugated diene polymer prepared using the same, and more particularly to a polymerization initiator which is a compound represented by the following formula 1, and a modified conjugated diene polymer prepared using the same: wherein R1 to R5 are each independently hydrogen or a C1-10 alkyl group or its carbanion; n? represents the number of negative charges of the carbanion and is 1? to 5?; M is a metal; and n is equal to the number of carbanions in R1 to R5.

POLYMERIZATION INITIATOR, MODIFIED-CONJUGATED DIENE POLYMER AND TIRE PRODUCED THEREFROM

The present disclosure relates to a polymerization initiator and a modified conjugated diene polymer prepared using the same, and more particularly to a polymerization initiator which is a compound represented by the following formula 1, and a modified conjugated diene polymer prepared using the same: wherein R1 to R5 are each independently hydrogen or a C1-10 alkylgroup or its carbanion; n? represents the number of negative charges of the carbanion and is 1? to 5?; M is a metal; and n is equal to the number of carbanions in R1 to R5.

Yttrium-catalyzed addition of benzylic C-H bonds of alkyl pyridines to olefins

Cationic half-sandwich yttrium alkyl complexes catalyze the ortho-selective benzylic C-H addition of dialkyl pyridines to various olefins, such as ethylene, 1-hexene, styrenes, and 1,3-conjugated dienes, to afford new alkylated and allylated pyridine derivatives (see scheme; Cp=C5Me 5). A cationic half-sandwich yttrium picolyl species, such as [CpY(2-CH2-6-CH3C5H3N)] +, has been confirmed to be a key active species in this transformation. Copyright

Catalytic Reactions of Pyridines. V. Alkylation of α-, β-, and γ-Picolines with Alcohols catalyzed by Ammonium Halides

A new method was found for the homogeneous liquid-phase alkylation of α-, β-, and γ-picolines with either methanol or ethanol.Addition of a catalytic amount of an ammonium halide to a mixture of a picoline and an alcohol resulted in a great increase in the yields of both side-chain and α-alkylated derivatives of the starting picoline when the reaction was carried out at 320-335 deg C in an atmosphere of nitrogen.The higher the reaction temperature, the greater the yields of side-chain alkylated derivatives became.In practice, this alkylation gave 2-ethylpyridine, and 2,6-lutidine from α-picoline with methanol, 3-ethylpyridine and 2,5-lutidine from β-picoline from methanol, 4-ethylpyridine and 2,4-lutidine from γ-picoline with methanol, 2-propylpyridine and 2-ethyl-6-methylpyridine from α-picoline with ethanol, 2-ethyl-5-methylpyridine from β-picoline with ethanol, and 4-propylpyridine and 2-ethyl-4-methylpyridine from γ-picoline with ethanol.Keywords-alkylation; catalyst; ammonium halide; α-picoline; β-picoline; γ-picoline; ethylpyridine; propylpyridine; methanol; ethanol