6-Chloro-5-(trifluoromethyl)pyridine-3-sulfonamide

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Reagent Code: #49770
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CAS Number 1228875-16-8

science Other reagents with same CAS 1228875-16-8

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Weight 260.6200 g/mol
Formula C₆H₄ClF₃N₂O₂S
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MDL Number MFCD18072465
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This chemical is primarily used in the synthesis of agrochemicals, particularly as an intermediate in the production of herbicides and pesticides. Its structure allows it to interact effectively with biological targets, making it valuable in developing compounds that control weed growth and protect crops from pests. Additionally, it finds application in pharmaceutical research, where it serves as a building block for creating molecules with potential therapeutic properties, such as anti-inflammatory or antimicrobial agents. Its chloro, trifluoromethyl, and sulfonamide groups contribute to its reactivity and biological activity, making it a versatile component in various chemical synthesis processes.

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inventory 100mg
10-20 days ฿13,014.00

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6-Chloro-5-(trifluoromethyl)pyridine-3-sulfonamide
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This chemical is primarily used in the synthesis of agrochemicals, particularly as an intermediate in the production of herbicides and pesticides. Its structure allows it to interact effectively with biological targets, making it valuable in developing compounds that control weed growth and protect crops from pests. Additionally, it finds application in pharmaceutical research, where it serves as a building block for creating molecules with potential therapeutic properties, such as anti-inflammatory or anti
This chemical is primarily used in the synthesis of agrochemicals, particularly as an intermediate in the production of herbicides and pesticides. Its structure allows it to interact effectively with biological targets, making it valuable in developing compounds that control weed growth and protect crops from pests. Additionally, it finds application in pharmaceutical research, where it serves as a building block for creating molecules with potential therapeutic properties, such as anti-inflammatory or antimicrobial agents. Its chloro, trifluoromethyl, and sulfonamide groups contribute to its reactivity and biological activity, making it a versatile component in various chemical synthesis processes.
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