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Structure of 16807-13-9
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3-Iodo-9H-carbazole is a bench-stable heterocyclic iodide featuring a carbazole core with a reactive iodine substituent at the 3-position. This compound serves as a key building block in cross-coupling chemistry, enabling efficient C–C bond formation under standard catalytic conditions. The electron-rich aromatic system enhances reactivity in palladium-mediated transformations, while the iodide group facilitates selective functionalization. Its stability and predictable reactivity make it well-suited for synthetic applications in organic electronics and pharmaceutical development.
3-Iodo-9H-carbazole serves as a versatile building block in transition-metal-catalyzed cross-coupling reactions, enabling efficient construction of biaryl and heteroaryl architectures. Its iodine substituent facilitates reliable Suzuki, Stille, and Negishi couplings under standard conditions. The carbazole core provides inherent stability and π-conjugation, making it valuable for synthesizing functional materials and pharmaceutical intermediates. Bench-stable and readily purified by column chromatography, it functions effectively in multi-step syntheses requiring robust functional group tolerance.
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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-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: