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Structure of 33255-13-9
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3,6-Dibromo-9-ethyl-9H-carbazole features two bromine substituents at the 3 and 6 positions of the carbazole core, enhancing electrophilic reactivity for cross-coupling transformations. The ethyl group at the 9-position improves solubility and modulates electronic properties, enabling efficient incorporation into conjugated polymers and functional materials.
3,6-Dibromo-9-ethyl-9H-carbazole serves as a versatile building block for the synthesis of functionalized carbazole derivatives. The dibromo substitution enables efficient Suzuki-Miyaura and Stille coupling reactions, facilitating the construction of conjugated polymers and bioactive heterocycles. The ethyl group at the 9-position enhances solubility and modulates electronic properties, while the bromine atoms offer high reactivity under standard palladium-catalyzed conditions. This compound exhibits excellent bench stability and is readily purified by column chromatography, making it well-suited for industrial R&D workflows in materials science and medicinal chemistry.
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GHS Pictogram :
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GHS No : GHS05,GHS07
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Signal Word : Danger
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UN#: 1759
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Class : 8
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Packing Group : Ⅲ
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Hazard Statements : H302-H318-H413
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Precautionary Statements : P264-P270-P273-P280-P330-P501
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Lot numbers can be found on the outside label of a product: