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Structure of 144981-85-1
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This fluorene derivative features a reactive iodine substituent at the 2-position, enabling efficient coupling in cross-coupling reactions. The electron-rich fluorene core enhances stability and solubility, while the dimethyl groups provide steric protection, minimizing side reactions. Ideal for constructing complex architectures in synthetic organic chemistry.
2-Iodo-9,9-dimethyl-9H-fluorene serves as a robust building block for Suzuki-Miyaura cross-coupling reactions, leveraging its stable fluorene core and iodine substituent for efficient C–C bond formation. The sterically hindered 9,9-dimethyl groups enhance bench stability and resist unwanted side reactions, while the iodo functionality exhibits high reactivity under standard palladium catalysis. This compound facilitates the synthesis of functionalized biaryls and complex heterocyclic systems relevant to pharmaceutical and materials chemistry.
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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: