65515-26-6

Basic information

• Product Name: Methyl 2,6-dimethoxypyridine-3-carboxylate
• Synonyms: Methyl 2,6-dimethoxypyridine-3-carboxylate;Methyl 2,6-diMethoxynicotinate
• CAS NO: 65515-26-6
• Molecular Formula: C9H11NO4
• Molecular Weight: 197.18794
• Mol File: 65515-26-6.mol
• Article Data: 6

Chemical Properties

• Appearance: /
• Storage Temp.: Inert atmosphere,Room Temperature
• CAS DataBase Reference: Methyl 2,6-dimethoxypyridine-3-carboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: Methyl 2,6-dimethoxypyridine-3-carboxylate(65515-26-6)
• EPA Substance Registry System: Methyl 2,6-dimethoxypyridine-3-carboxylate(65515-26-6)

Safety Data

• HazardClass: IRRITANT
• Hazardous Substances Data: 65515-26-6(Hazardous Substances Data)

Usage

General Description

"Methyl 2,6-dimethoxypyridine-3-carboxylate" is a chemical compound with the molecular formula C10H11NO4. It is an ester of 2,6-dimethoxypyridine-3-carboxylic acid and methanol. Methyl 2,6-dimethoxypyridine-3-carboxylate is commonly used as an intermediate in the synthesis of pharmaceuticals and agrochemicals due to its unique chemical properties. It is also known for its potential applications in the field of medicinal chemistry, specifically in the development of new drugs. Additionally, it can be used as a building block in organic synthesis, contributing to the creation of various compounds with important biological activities.

InChI:InChI=1S/C9H11NO4/c1-12-7-5-4-6(9(11)14-3)8(10-7)13-2/h4-5H,1-3H3

Upstream product

• 124-41-4 sodium methylate 
• 117671-02-0 methyl 2,6-difluoro-3-pyridinecarboxylate 
• 65515-28-8 methyl 2,6-dichloronicotinate 
• 38496-18-3 2,6-dichloropyridine-3-carboxylic acid 
• 171178-50-0 2,6-difluoronicotinic acid 
• 67-56-1 methanol 
• 562840-47-5 (2,6-dimethoxypyridin-3-yl)methanol 

Downstream Products

• 562840-46-4 2,6-dimethoxynicotinic acid ethyl ester 

Relevant articles and documents

A “universal” catalyst for aerobic oxidations to synthesize (hetero)aromatic aldehydes, ketones, esters, acids, nitriles, and amides

Functionalized (hetero)aromatic compounds are indispensable chemicals widely used in basic and applied sciences. Among these, especially aromatic aldehydes, ketones, carboxylic acids, esters, nitriles, and amides represent valuable fine and bulk chemicals, which are used in chemical, pharmaceutical, agrochemical, and material industries. For their synthesis, catalytic aerobic oxidation of alcohols constitutes a green, sustainable, and cost-effective process, which should ideally make use of active and selective 3D metals. Here, we report the preparation of graphitic layers encapsulated in Co-nanoparticles by pyrolysis of cobalt-piperazine-tartaric acid complex on carbon as a most general oxidation catalyst. This unique material allows for the synthesis of simple, functionalized, and structurally diverse (hetero)aromatic aldehydes, ketones, carboxylic acids, esters, nitriles, and amides from alcohols in excellent yields in the presence of air.

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The present invention relates to novel PPAR agonist compounds as well as pharmaceutical compositions containing them. The compounds according to the invention are of quite particular therapeutic interest, notably for treating diabetes and/or dyslipidemias, as well as for preventing cardiovascular pathologies.

An efficient synthesis of 5-bromo-2-methoxy-6-methylaminopyridine-3-carboxylic acid

An efficient synthesis of 5-bromo-2-methoxy-6-methylaminopyridine-3-carboxylic acid (1), a carboxylic acid moiety of a potent dopamine D2 and D3 and serotonin-3 (5-HT3) receptors antagonist, (R)-5-bromo-N-(1-ethyl-4-methyl