88579-63-9

Usage

Uses

Due to the limited information available on the applications of 2,6-Dichloropyridine-4-methylamine, it is not possible to list specific uses or industries where it is employed. However, given its role in the synthesis of various organic compounds, it can be inferred that it may be used as a chemical intermediate in the production of pharmaceuticals, agrochemicals, or other specialty chemicals. Further research and information from reliable sources would be required to confirm its specific applications and industries of use.

InChI:InChI=1/C6H6Cl2N2/c7-5-1-4(3-9)2-6(8)10-5/h1-2H,3,9H2

Upstream product

• 42521-08-4 2,6-dichloroisonicotinoyl chloride 
• 5398-44-7 2,6-dichloropyridine-4-carboxylic acid 
• 89281-13-0 2,6-dichloropyridine-4-carboxamide 
• 32710-65-9 2,6-dichloro-4-cyanopyridine 

Downstream Products

• 101990-69-6 (2,6-dichloropyridin-4-yl)methanol 

Relevant academic research and scientific papers

Pyridine methylamine compound and preparation method thereof

The invention provides a pyridine methylamine compound and a preparation method thereof. The preparation method comprises the steps that tetrahydrofuran and sodium borohydride are sequentially added into a cyanopyridine compound, then an iodine-containing tetrahydrofuran solution is dropwise added, a reaction is conducted at the temperature of 20-30 DEG C, and after dropwise adding is completed, stirring is carried out continuously; after the reaction is finished, methanol is added for refluxing, extracting and spin-drying are carried out to obtain the pyridine methylamine compound; wherein a functional group in the cyanopyridine compound is selected from chlorine, bromine, methyl, ethyl, amino or hydrogen; according to the preparation method, high-temperature and high-pressure special equipment does not need to be used, so that the preparation method is relatively safe, and dangerous accidents such as explosion and fire disasters are avoided; besides, the preparation method is relatively environment-friendly, recycling treatment of hazardous waste (used Raney nickel) is not involved, the economic benefit is relatively high, borane generated by the synthesis method is converted into boric acid esters in the post-treatment process, the treatment cost is low, and the harm to the environment is much small.