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Structure of 1053657-15-0
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tert-Butyl 4-chloro-5H-pyrrolo[3,4-d]pyrimidine-6(7H)-carboxylate features a sterically hindered tert-butyl ester paired with a chlorine-substituted pyrrolopyrimidine core. This bench-stable scaffold integrates readily into heterocyclic synthesis, enabling efficient access to bioactive purine analogs and kinase inhibitor precursors under standard conditions.
tert-Butyl 4-chloro-5H-pyrrolo[3,4-d]pyrimidine-6(7H)-carboxylate serves as a versatile building block for purine and pyrrolopyrimidine-based scaffolds. The chloro group enables direct nucleophilic substitution in late-stage functionalization, while the tert-butyl ester offers bench stability and facile deprotection under mild acidic conditions. This compound facilitates efficient access to biologically relevant heterocycles via Pd-catalyzed coupling or amine displacement reactions, making it valuable in medicinal chemistry and API synthesis 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
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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: