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Structure of 226386-47-6
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2-Bromo-4,5,6,7-tetrahydrothieno[3,2-c]pyridine features a fused thienopyridine core with a bromine substituent at the 2-position, enabling direct functionalization in cross-coupling reactions. The saturated thiophene ring enhances solubility and stability under standard conditions, while the electron-deficient heterocycle facilitates transition metal-catalyzed transformations. This scaffold serves as a key building block for bioactive molecules and advanced materials.
2-Bromo-4,5,6,7-tetrahydrothieno[3,2-c]pyridine serves as a versatile scaffold for constructing biologically relevant heterocycles, enabling efficient Pd-catalyzed cross-coupling reactions. The bromine substituent provides high reactivity in standard Suzuki, Stille, and Negishi couplings, while the saturated thienopyridine core offers enhanced stability and solubility. Its functional group tolerance facilitates downstream derivatization in medicinal chemistry workflows.
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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
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Precautionary Statements : P264-P270-P280-P302+P352-P330-P362+P364-P501
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Lot numbers can be found on the outside label of a product: