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Structure of 612499-04-4
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(5-Bromothiophen-2-yl)methanamine features a brominated thiophene ring linked to a primary amine group, enabling direct incorporation into heterocyclic scaffolds. This bench-stable derivative serves as a key building block for pharmaceutical intermediates and functional materials, offering high reactivity in cross-coupling and cyclization reactions under standard conditions.
(5-Bromothiophen-2-yl)methanamine serves as a versatile building block for the synthesis of biologically active heterocycles and functionalized arylamines. Its bromine substituent enables palladium-catalyzed cross-coupling reactions, while the primary amine group facilitates direct derivatization or incorporation into pharmaceutical scaffolds. The compound exhibits good bench stability and is compatible with standard purification protocols, making it well-suited for iterative synthetic strategies in medicinal chemistry and process development.
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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: