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Structure of 24209-95-8
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9-(4,6-Dichloro-1,3,5-triazin-2-yl)-9H-carbazole is a highly reactive triazine-based coupling reagent featuring two chlorine atoms at the 4- and 6-positions of the triazine ring. This configuration enables efficient activation of nucleophiles in amide bond formation and bioconjugation workflows. The electron-deficient triazine moiety readily engages with amines and hydroxyl groups under mild conditions. The carbazole scaffold provides enhanced stability and solubility in organic solvents. This compound serves as a robust linker in the synthesis of functionalized biomolecules and materials.
9-(4,6-Dichloro-1,3,5-triazin-2-yl)-9H-carbazole serves as a versatile bifunctional building block for the synthesis of conjugated materials and functionalized heterocycles. The electrophilic triazine moiety enables efficient coupling with nucleophiles such as amines and alcohols under mild conditions, while the carbazole core provides robust stability and favorable electronic properties. Its bench-stable nature and clean reaction profile facilitate straightforward purification and scalability in synthetic workflows.
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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-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: