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Structure of 119999-22-3
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6-Bromo-1,1,4,4,7-pentamethyl-1,2,3,4-tetrahydronaphthalene features a sterically shielded tetrahydronaphthalene core with a bromine substituent at the 6-position. This configuration enhances stability and directs regioselective transformations in cross-coupling reactions. The molecule’s electron-rich aromatic system facilitates efficient palladium-catalyzed functionalizations under mild conditions.
6-Bromo-1,1,4,4,7-pentamethyl-1,2,3,4-tetrahydronaphthalene serves as a sterically hindered aryl bromide building block for palladium-catalyzed cross-coupling reactions. Its electron-rich tetrahydronaphthalene core enhances stability and reactivity in Suzuki, Stille, and Negishi couplings. The methyl substituents provide robust protection against undesired side reactions, enabling clean transformations with broad functional group tolerance. This compound facilitates efficient construction of complex alkylated aromatic scaffolds in medicinal chemistry and materials synthesis.
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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: