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Structure of 865472-04-4
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7-Bromo-1,2,3,4-tetrahydronaphthalen-1-amine features a brominated tetrahydronaphthalene core with a primary amine at the 1-position, enabling direct functionalization in synthetic routes. The electron-rich aromatic system enhances reactivity in cross-coupling processes, while the amine group provides a handle for derivatization. This bench-stable scaffold serves as a key intermediate in medicinal chemistry and materials synthesis.
7-Bromo-1,2,3,4-tetrahydronaphthalen-1-amine serves as a versatile scaffold for medicinal chemistry and process development, enabling direct functionalization at the aromatic ring and amine handle. Its bench-stable nature and compatibility with standard coupling reactions facilitate efficient derivatization. The bromo group supports palladium-catalyzed cross-coupling, while the primary amine allows for amide formation, reductive amination, or sulfonamide synthesis—key transformations in API lead optimization and heterocycle construction.
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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: