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Structure of 1354777-44-8
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5-Bromo-1H-1,2,3-benzotriazole-7-carboxylic acid features a brominated benzotriazole core paired with a carboxylic acid group, enabling direct conjugation or derivatization in synthetic workflows. The electron-deficient triazole ring enhances reactivity in transition metal-catalyzed coupling reactions, while the carboxylic acid facilitates salt formation and purification. This compound serves as a robust scaffold for bioactive molecule synthesis and functional materials development under standard conditions.
5-Bromo-1H-1,2,3-benzotriazole-7-carboxylic acid serves as a versatile building block for the synthesis of functionalized heterocycles and bioactive molecules. The bromo group enables palladium-catalyzed cross-coupling reactions, while the carboxylic acid facilitates amide formation or derivatization. Its stability under standard reaction conditions and compatibility with diverse functional groups make it a practical reagent for medicinal chemistry and materials science applications.
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GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H302-H315-H319-H335
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Precautionary Statements : P261-P280-P302+P352
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Lot numbers can be found on the outside label of a product: