4-Chloro-1-methyl-3-nitropyridin-2(1H)-one

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Reagent Code: #47050
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CAS Number 719268-89-0

science Other reagents with same CAS 719268-89-0

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Weight 188.5685 g/mol
Formula C₆H₅ClN₂O₃
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MDL Number MFCD25949141
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This chemical is primarily used in the field of organic synthesis, where it serves as a key intermediate in the production of various pharmaceuticals and agrochemicals. Its structure allows for further functionalization, making it valuable in the development of compounds with potential biological activity. Researchers often utilize it to create derivatives that can be tested for their efficacy in treating diseases or as active ingredients in pesticides. Additionally, it plays a role in the synthesis of complex molecules in medicinal chemistry, contributing to the discovery of new drugs. Its nitro and chloro groups make it a versatile building block in chemical reactions, enabling the creation of diverse molecular architectures.

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inventory 250mg
10-20 days ฿9,531.00

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4-Chloro-1-methyl-3-nitropyridin-2(1H)-one
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This chemical is primarily used in the field of organic synthesis, where it serves as a key intermediate in the production of various pharmaceuticals and agrochemicals. Its structure allows for further functionalization, making it valuable in the development of compounds with potential biological activity. Researchers often utilize it to create derivatives that can be tested for their efficacy in treating diseases or as active ingredients in pesticides. Additionally, it plays a role in the synthesis of c

This chemical is primarily used in the field of organic synthesis, where it serves as a key intermediate in the production of various pharmaceuticals and agrochemicals. Its structure allows for further functionalization, making it valuable in the development of compounds with potential biological activity. Researchers often utilize it to create derivatives that can be tested for their efficacy in treating diseases or as active ingredients in pesticides. Additionally, it plays a role in the synthesis of complex molecules in medicinal chemistry, contributing to the discovery of new drugs. Its nitro and chloro groups make it a versatile building block in chemical reactions, enabling the creation of diverse molecular architectures.

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