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Structure of 1378816-68-2
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7-Bromo-5H-pyrrolo[3,2-d]pyrimidine is a bench-stable heterocyclic building block featuring a bromine substituent at the 7-position, enabling direct functionalization in cross-coupling reactions. The electron-deficient pyrimidine core pairs effectively with nucleophilic partners, facilitating rapid access to advanced purine analogs and kinase-targeted pharmaceutical scaffolds under standard conditions.
7-Bromo-5H-pyrrolo[3,2-d]pyrimidine serves as a versatile building block for purine-based scaffolds, enabling efficient late-stage functionalization via Pd-catalyzed cross-coupling reactions. Its bromine substituent exhibits high reactivity in Suzuki, Stille, and Negishi couplings, while the fused heterocyclic core provides excellent bench stability and compatibility with diverse reaction conditions. This compound facilitates rapid access to biologically relevant frameworks in 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-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: