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Structure of 1363381-59-2
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1-(4-Chloro-7H-pyrrolo[2,3-d]pyrimidin-5-yl)ethanone is a bench-stable heterocyclic ketone featuring a chlorinated pyrrolopyrimidine core. This compound integrates readily into medicinal chemistry campaigns, serving as a key intermediate for kinase inhibitors and nucleoside analogs. The acetyl group enables direct derivatization via nucleophilic addition or reductive amination.
1-(4-Chloro-7H-pyrrolo[2,3-d]pyrimidin-5-yl)ethanone serves as a versatile building block in medicinal chemistry, enabling direct functionalization at the C5 position of the pyrrolopyrimidine core. Its acetyl group facilitates electrophilic substitution and transition-metal-catalyzed coupling reactions, while the chloro substituent supports palladium-mediated cross-couplings. The compound exhibits excellent bench stability and compatibility with standard purification methods, making it well-suited for iterative synthesis of kinase inhibitors and other heterocyclic APIs.
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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: