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Usage

Uses

Used in Pharmaceutical Industry:
ETHYL 2,4-DICHLORO-6-METHYLPYRIDINE-3-CARBOXYLATE is used as an intermediate in the synthesis of various pharmaceuticals for its ability to contribute to the development of new drugs.
Used in Agrochemical Industry:
ETHYL 2,4-DICHLORO-6-METHYLPYRIDINE-3-CARBOXYLATE is used as an active ingredient in the formulation of insecticides and herbicides, leveraging its insecticidal and pesticidal properties to control pests in agricultural settings.
Used in Fine Chemicals Production:
ETHYL 2,4-DICHLORO-6-METHYLPYRIDINE-3-CARBOXYLATE is used as a building block in the production of fine chemicals, playing a crucial role in the synthesis of specialty compounds for various applications.

InChI:InChI=1/C9H9Cl2NO2/c1-3-14-9(13)7-6(10)4-5(2)12-8(7)11/h4H,3H2,1-2H3

Upstream product

• 10350-10-4 ethyl 2,4-dihydroxy-6-methylnicotinate 
• 10350-10-4 ethyl 1,2-dihydro-2-oxo-4-hydroxy-6-methylpyridine-3-carboxylate 
• 105-53-3 diethyl malonate 

Downstream Products

• 947146-50-1 ethyl 2,4-dibenzylamino-6-methyl-pyridine-3-carboxylate 
• 1315469-34-1 [2-chloro-4-(2,5-dichloro-phenoxy)-6-methyl-pyridin-3-yl]-(4-cyclopropyl-3,4-dihydro-2H-quinoxalin-1-yl)-methanone 
• 1315469-67-0 lithium 2-chloro-4-(2,5-dichloro-phenoxy)-6-methyl-nicotinate 
• 38367-36-1 2,4-dichloro-6-methyl-3-pyridinecarbonitrile 
• 1347759-32-3 C₂₄H₂₅ClN₆O₂ 
• 1347759-31-2 2-(1-(4-methoxybenzyl)-6-methyl-4-(tetrahydro-2H-pyran-4-ylamino)-1H-pyrazolo[4,3-c]pyridin-3-yl)-N,N-dimethylisonicotinamide 
• 1347759-30-1 2-(1-(4-methoxybenzyl)-6-methyl-4-(tetrahydro-2H-pyran-4-ylamino)-1H-pyrazolo[4,3-c]pyridine-3-yl)isonicotinic acid 
• 1347759-29-8 methyl 2-(1-(4-methoxybenzyl)-6-methyl-4-(tetrahydro-2H-pyran-4-ylamino)-1H-pyrazolo[4,3-c]pyridin-3-yl)isonicotinate 
• 1347759-28-7 1-(4-methoxybenzyl)-6-methyl-N-(tetrahydro-2H-pyran-4-yl)-3-(trimethylstannyl)-1H-pyrazolo[4,3-c]pyridin-4-amine 
• 1347759-27-6 3-iodo-1-(4-methoxybenzyl)-6-methyl-N-(tetrahydro-2H-pyran-4-yl)-1H-pyrazolo[4,3-c]pyridin-4-amine 
• 1347759-26-5 4-chloro-3-iodo-1-(4-methoxybenzyl)-6-methyl-1H-pyrazolo[4,3-c]pyridine 
• 1159828-70-2 4-chloro-6-methyl-1H-pyrazolo[4,3-c]pyridine 
• 1347759-24-3 3-iodo-4-(tetrahydro-2H-pyran-4-yloxy)-1-trityl-1H-pyrazolo[4,3-c]pyridine-6-carbonitrile 
• 1347759-23-2 3-iodo-4-(tetrahydro-2H-pyran-4-yloxy)-1-trityl-1H-pyrazolo[4,3-c]pyridine-6-carbaldehyde 

Relevant academic research and scientific papers

SULFONYL AMIDE DERIVATIVES FOR THE TREATMENT OF ABNORMAL CELL GROWTH

The present invention relates to a compound of the formula I wherein R1 to R6, A, B, n and m are as defined herein. Such novel sulfonyl amide derivatives are useful in the treatment of abnormal cell growth, such as cancer, in mammals. This invention also relates to a method of using such compounds in the treatment of abnormal cell growth in mammals, especially humans, and to pharmaceutical compositions containing such compounds.

Thermal Cyclization of 3-Acyl-4-azidopyridines to Isoxazolo[4,3-c]pyridines

4-Azidopyridines such as 3-acetyl-4-azido-2-pyridones 3 or 4-azido-3-ethoxycarbonylpyridine 7 with reactive ortho-acyl substituents were obtained from the 4-hydroxy-2-pyridones 1, resp. 5 via 4-tosyloxy-2-pyridones 2 or the 2,4-dichloropyridine 6. DSC-ass

An Easy and Convenient Synthesis of 6-Methyl-4(1H)-pyridone-3-carboxylic Acid

A new and easy synthesis of 6-methyl-4(1H)-pyridone-3-carboxylic acid (5), an important component of broad spectrum cephalosporins, is described.It starts from the readily available ethyl 4-hydroxy-6-methyl-2(1H)-pyridone-3-carboxylate (1), which is treated with phosphoryl chloride to give ethyl 2,4-dichloro-6-methylpyridine-3-carboxylate (2).Selective substitution of the chlorine in 4-position with alkoxide ion leads to the 4-alkoxypyridine derivatives 3.Hydrogenolysis of 3 affords ethyl 4-alkoxy-6-methyl-pyridine-3-carboxylates 4; which are hydrolysed to 5 in one step.

Aza Analogues of Lucanthone: Synthesis and Antitumor and Bactericidal Properties

Three types of aza analogues of lucanthone were synthesized for evaluation as antitumor drugs.None of the compounds was found to have significant cytotoxic effects either on Friend tumor cells or on L1210 leukemia cells.However, one of the target compound