468718-67-4

Usage

Uses

Used in Pharmaceutical Industry:
2-Pyridinamine,3-chloro-N-methyl-(9CI) is used as an intermediate in the synthesis of various pharmaceutical compounds. Its unique structure and properties allow it to be incorporated into the development of new drugs, potentially leading to the creation of novel therapeutic agents.
Used in Agrochemical Industry:
In the agrochemical industry, 2-Pyridinamine,3-chloro-N-methyl-(9CI) is utilized as a building block for the synthesis of agrochemicals, such as pesticides and herbicides. Its chemical properties enable it to be a key component in the development of effective and targeted agrochemical products.
Used in Material Science:
2-Pyridinamine,3-chloro-N-methyl-(9CI) may have potential applications in the development of new materials and technologies. Its ability to form hydrogen bonds and its unique structure can contribute to the creation of innovative materials with specific properties for various applications.
It is important to handle 2-Pyridinamine,3-chloro-N-methyl-(9CI) with care and be aware of its potential hazards, as it may pose risks to human health and the environment if not properly managed.

Upstream product

• 468718-63-0 N-(3-chloro-4-trimethylsilylpyridin-2-yl)-N-methylamine 
• 468718-72-1 2-amino-3-chloro-4-trimethylsilylpyridine 
• 468718-70-9 N-(3-chloro-4-trimethylsilylpyridin-2-yl)-2,2-dimethylpropanamide 
• 2402-77-9 2,3-dichloro-pyridine 
• 74-89-5 methylamine 

Relevant academic research and scientific papers

SUBSTITUTED HETEROCYCLIC INHIBITORS OF PTPN11

The present invention relates to compounds which may be useful as inhibitors of PTPN11 for the treatment or prevention of cancer and other PTP-mediated diseases. Disclosed herein are new compounds and compounds based on pyrazolopyrazines and their applica

Iridium- and rhodium-catalyzed dehydrogenative silylations of C(sp 3) - H bonds adjacent to a nitrogen atom using hydrosilanes

Now that is just silylated: In the presence of iridium or rhodium catalysts, C(sp3) - H bonds adjacent to a nitrogen atom were silylated by the aid of a pyridine-directing group. In iridium catalysis, a hydrogen-trapping reagent such as norbornene or tert-butylethylene, which is usually required in late transition-metal-catalyzed dehydrogenative coupling reactions, was not required. In rhodium catalysis, however, 1 equivalent of COD (1,5-cyclooctadiene) was necessary to induce higher conversion. Copyright

BENZAMIDE DERIVATIVE OR SALT THEREOF

There is provided a compound having a capsaicin receptor VR1 inhibitory activity and useful as a therapeutic agent for various pains including inflammatory pain and neurogenic pain, migraine, cluster headache, bladder diseases including overactive bladder

Hetarynic synthesis and chemical transformation of dihydrodipyridopyrazines

Unprecedented dihydrodipyridopyrazines were easily obtained by hetarynic dimerization of 2-alkylamino-3-halogenopyridines in the presence of the complex base NaNH2-tBuONa. Derivatizations of the new heterocycles are described. The anticancer ac