204378-41-6

Usage

Uses

Used in Agricultural Industry:
Methyl 6-chloro-4-methoxypicolinate is used as a pesticide or herbicide for its ability to inhibit certain enzymes involved in plant growth, thereby controlling or preventing unwanted vegetation.
Used in Pharmaceutical Industry:
Methyl 6-chloro-4-methoxypicolinate serves as a building block for the synthesis of more complex organic molecules, contributing to the development of new pharmaceutical compounds.
Used in Research Applications:
In research settings, methyl 6-chloro-4-methoxypicolinate is utilized for its potential in the synthesis of novel organic compounds, aiding in the advancement of chemical and material sciences.

InChI:InChI=1/C8H8ClNO3/c1-12-5-3-6(8(11)13-2)10-7(9)4-5/h3-4H,1-2H3

Upstream product

• 29681-43-4 methyl 4-methoxypicolinate 
• 86251-47-0 4-methoxy-2-(methoxycarbonyl)pyridine 1-oxide 
• 88912-25-8 4,6-dichloro-2-pyridinecarboxylic acid 
• 67-56-1 methanol 
• 98273-19-9 methyl 4,6-dichloropyridine-2-carboxylate 
• 124-41-4 sodium methylate 

Downstream Products

• 1186606-54-1 (S)-N-(3-(2-ethyl-4-(5-(4-methoxy-6-(pentan-3-yl)pyridin-2-yl)-1,2,4-oxadiazol-3-yl)-6-methylphenoxy)-2-hydroxypropyl)-2-hydroxyacetamide 
• 88912-21-4 4-methoxy-6-chloro picolinic acid 

Relevant academic research and scientific papers

CD38 INHIBITORS

One embodiment of the invention is a compound represented by Formula I: or a pharmaceutically acceptable salt thereof. The variables in Formula I are defined herein. Compounds of Formula I are CD38 inhibitors, which can be used to treat a disease or condition in a subject that benefits from an increase in NAD+ or to treat a mitochondrial disorder in a subject.

2-chloroadenine derivative as well as preparation method and application thereof

The invention belongs to the technical field of medicinal chemistry, and particularly relates to a 2-chloroadenine derivative as well as a preparation method and application thereof. The 2-chloroadenine derivative provided by the invention has a good inhibition effect on phosphodiesterase type 8, also has relatively good liver microsome stability and patent medicine property, can be applied to preparation of medicines for treating and/or preventing diseases related to phosphodiesterase type 8, and has relatively good development potential, and the selectable range of drugs for treating phosphodiesterase 8 type related diseases is increased.

PYRIDIN-2-YL DERIVATIVES AS IMMUNOMODULATING AGENTS

The invention relates to pyridine derivatives of Formula (I), wherein A, R1, R2, R3, R4, R5, R6 and R7 are as described in the description, their preparation and their use as pharmaceutically active compounds. Said compounds particularly act as immunomodulating agents.

N-(phenylsulfonyl)picolinamide derivatives, process for producing the same, and herbicide

A herbicide containing as the active ingredient an N-(henylsulfonyl)picolinamide derivative represented by general formula (I) wherein X reprcsents a halogeno, a C1-4 alkyl, a C1-4 haloalkyl, a C1-4 alkoxy, a C1-4 haloalkoxy, a (C1-4 alkoxy)carbonyl, a [di(C1-4 alkyl)amino]sulfonyl, an [N—(C1-4 alkyl)-N—(C1-4 alkoxy)amino]sulfonyl, a (C1-4 alkylamino)sulfonyl, a C1-4 alkylthio, a C1-4 alkylsulfinyl, a C1-4 alkylsulfonyl, or nitro; n is an integer of 0 to 5; Y represets a halogeno, a C1-4 alkyl, a C1-4 haloalkyl, a C1-4 alkoxy, C1-4 haloalkoxy, a C1-4 alkylthio, a C1-4 haloalkylthio, amino, a C1-4 alkylamino, a di(C1-4 alkyl)amino, a (C1-4 alkoxy) C1-4 alkyl, a (C1-4 alkylthio) C1-4 alkyl, or nitro; and m is an integer of 0 to 4. This active ingredient is synthesized by condensing a substituted picolinic acid with a substituted benzenesulfonamide under dehydration, or by reacting the phenyl ester of a substituted picolinic acid with a substituted benzenesulfonamide in the presence of a basic compound.