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Structure of 175791-49-8
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5-Bromo-7H-pyrrolo[2,3-d]pyrimidine features a brominated pyrrolopyrimidine core with high electron deficiency, enabling direct functionalization in cross-coupling reactions. This bench-stable heterocycle integrates efficiently into kinase inhibitor scaffolds and other bioactive molecules, offering enhanced reactivity and structural rigidity for medicinal chemistry applications.
5-Bromo-7H-pyrrolo[2,3-d]pyrimidine serves as a versatile building block in heterocyclic synthesis, enabling efficient late-stage functionalization via palladium-catalyzed cross-coupling reactions. The bromine substituent provides high reactivity in Suzuki, Stille, and Negishi couplings, facilitating the construction of biologically relevant scaffolds. Its stability under standard reaction conditions and compatibility with diverse functional groups make it a practical choice for medicinal chemistry and process development 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-H335-H312-H332
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Precautionary Statements : P260-P261-P264-P270-P271-P280-P301+P310-P302+P352-P304+P340-P304+P341-P305+P351+P338-P312-P330-P332+P313-P337+P313-P362+P364-P363-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: