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Structure of 22276-95-5
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5-Bromo-4-chloro-7H-pyrrolo[2,3-d]pyrimidine delivers a highly reactive heterocyclic scaffold for medicinal chemistry applications. This electron-deficient purine analog integrates readily into kinase inhibitors and nucleoside analogs, offering enhanced metabolic stability. The bromo and chloro substituents enable efficient cross-coupling transformations under mild conditions, facilitating rapid diversification of core structures.
5-Bromo-4-chloro-7H-pyrrolo[2,3-d]pyrimidine serves as a versatile building block in the synthesis of purine-based scaffolds. Its orthogonal halogenation pattern enables sequential cross-coupling reactions with high regiocontrol, facilitating the construction of biologically relevant heterocycles. The compound exhibits excellent bench stability and is compatible with standard Pd-catalyzed transformations, simplifying purification and scale-up in medicinal chemistry campaigns.
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GHS Pictogram :
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GHS No : GHS06
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Signal Word : Danger
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UN#: 2811
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Class : 6.1
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Packing Group : Ⅲ
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Hazard Statements : H301
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Precautionary Statements : P264-P270-P330-P405-P501
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Lot numbers can be found on the outside label of a product: