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Structure of 1784280-46-1
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2-Bromothieno[3,2-c]pyridin-4-amine features a fused thienopyridine core with a bromine atom at the 2-position and an amine group at the 4-position. This scaffold delivers a rigid, electron-deficient heterocycle ideal for coupling reactions in medicinal chemistry. The bromine serves as a versatile handle for palladium-catalyzed transformations, while the amine enables direct derivatization or salt formation. Bench-stable under standard conditions, it integrates efficiently into diverse molecular architectures.
2-Bromothieno[3,2-c]pyridin-4-amine serves as a versatile building block for heterocyclic synthesis, enabling palladium-catalyzed cross-coupling reactions due to its bromine substituent and electron-rich nitrogen framework. The molecule exhibits bench stability, facilitates straightforward purification, and functions effectively in the construction of complex scaffolds relevant to medicinal chemistry and materials science.
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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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: