67367-26-4

Usage

Uses

Used in Pharmaceutical Synthesis:
METHYL 2-METHOXYNICOTINATE is used as an intermediate in the synthesis of pharmaceuticals for its potential as an anti-inflammatory agent, contributing to the development of treatments for various inflammatory conditions.
Used in Agrochemical Production:
In the agrochemical industry, METHYL 2-METHOXYNICOTINATE is used as a precursor in the production of various agrochemicals, leveraging its chemical properties to enhance crop protection and yield.
Used in Food and Beverage Industry:
METHYL 2-METHOXYNICOTINATE is used as a flavoring agent in the food and beverage industry, capitalizing on its fruity scent to impart unique and appealing flavors to a range of products.
Used in Skincare and Cosmetic Products:
METHYL 2-METHOXYNICOTINATE is used as an antioxidant in skincare and cosmetic products, benefiting formulations with its ability to protect against oxidative stress and potentially improve skin health and appearance.
Used in Neurological Disorder Treatment:
In the medical field, METHYL 2-METHOXYNICOTINATE is used as a component in treatments for neurological disorders, owing to its potential therapeutic effects on the nervous system.

Upstream product

• 67-56-1 methanol 
• 93-60-7 methyl 3-pyridinecarboxylate 
• 35905-85-2 2-bromonicotinic acid 

Downstream Products

• 162046-62-0 2-methoxy-pyridin-3-ylmethyl chloride 
• 884501-79-5 1-(4-methoxy-3-methylphenyl)-3-(2-methoxypyridin-3-yl)propane-1,3-dione 
• 884500-72-5 2-(4-hydroxyphenyl)-4H-pyrano[2,3-b]pyridin-4-one 
• 884500-75-8 2-(3-fluoro-4-hydroxyphenyl)-4H-pyrano[2,3-b]pyridin-4-one 
• 884500-82-7 2-(4-methoxyphenyl)-4H-pyrano[2,3-b]pyridine-4-one 
• 884501-05-7 4-(4-oxo-4H-pyrano[2,3-b]pyridine-2-yl)phenyl acetate 
• 884502-26-5 C₁₇H₁₃NO₄ 
• 884502-27-6 C₁₇H₁₂BrNO₄ 
• 1083168-93-7 methyl 2-methoxy-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine-3-carboxylate 

Relevant academic research and scientific papers

Synthesis of 9,9′-Spirobifluorenes and 4,5-Diaza-9,9′-spirobifluorenes and Their Application as Affinity Materials for Quartz Crystal Microbalances

Two different classes of aza analogues of 9,9′-spirobifluorenes have been synthesized. These were obtained by either furnishing the spirobifluorene with additional pyridyl moieties or by installing the aza function directly into the spirobifluorene core. These structurally rigid compounds were then evaluated as affinity materials for quartz crystal microbalances and proved to be highly potent for the detection of volatile organic compounds.

Multiple Paths for Photo-alkylation and -alkoxylation of 3-Pyridinecarboxylic Ester in Alcohol. Simultaneous Contribution of Several Kinds of Excited States

UV-irradiation of methyl 3-pyridinecarboxylate (1) in acidic alcoholic solutions brings about the alkoxylation and alkylation at the pyridine ring.Photoalkylation occurs in several paths: 1) alkylation initiated by the triplet ?-?* state, 2) alkylation initiated by the triplet n-?* state of the carbonyl moiety of the ester group, 3) alkylation initiated by exciplex between a free base form of 1 and a pyridinium form of 1, and 4) alkylation promoted by chloride ions.Photoalkoxylation originates from a singlet excited state of 1.In the photoreactions of 1 in strongly a cidic methanolic solutions acidified with H2SO4, three kinds of excited states (two kinds of triplet states for alkylation and a singlet state for alkoxylation) contribute simultaneously.

MULTIPLE PATHS FOR PHOTOALKYLATION OF PYRIDINECARBOXYLIC ESTERS IN ALCOHOLS

Photochemical substitution of ring hydrogen of pyridinecarboxylic esters by alkyl groups derived from solvent alcohols occurs in several paths: 1) alkylation initiated by excited carbonyl moiety of the ester group and 2) alkylation initiated by the excitation of the ?-electronic system of the pyridine ring.In the photoreaction of methyl 3-pyridinecarboxylate in acidic methanol, three types of excited state (two triplet states for alkylation and a singlet state for alkoxylation) contribute simultaneously.