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Structure of 22179-72-2
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4-Fluorobenzothioamide features a fluorinated aromatic ring paired with a thioamide functional group, delivering enhanced electronic effects and metabolic stability. This combination enables direct incorporation into heterocyclic scaffolds and facilitates conjugation in medicinal chemistry workflows. The compound exhibits good solubility in common organic solvents and maintains stability under standard bench conditions.
4-Fluorobenzothioamide serves as a versatile building block in medicinal chemistry, enabling the construction of heterocyclic scaffolds through cyclization reactions. Its fluorinated aryl moiety enhances metabolic stability and modulates electronic properties, while the thioamide group provides reliable reactivity in amide bond formation and transition metal-catalyzed coupling processes. Bench-stable and readily purified by recrystallization, it functions effectively in multi-step syntheses requiring functional group tolerance and predictable reactivity.
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GHS Pictogram :
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GHS No : GHS06
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Signal Word : Danger
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UN#: 2811
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Class : 6.1
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Packing Group : Ⅲ
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Hazard Statements : H301
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Precautionary Statements : P264-P270-P330-P405-P501
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Lot numbers can be found on the outside label of a product: