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Structure of 2351929-82-1
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2-Chloro-3-methyl-3,5-dihydro-4H-pyrrolo[3,2-d]pyrimidin-4-one features a sterically hindered, electron-deficient pyrrolopyrimidinone core that integrates readily into heterocyclic scaffolds. This bench-stable compound serves as a key intermediate in medicinal chemistry, enabling efficient access to kinase inhibitors and nucleoside analogs under standard conditions.
2-Chloro-3-methyl-3,5-dihydro-4H-pyrrolo[3,2-d]pyrimidin-4-one serves as a versatile building block for heterocyclic synthesis, enabling efficient access to pyrrolopyrimidine scaffolds prevalent in medicinal chemistry. Its reactive chloro group facilitates nucleophilic substitution under mild conditions, while the methyl and carbonyl functionalities provide orthogonal handles for further functionalization. The compound exhibits good bench stability and is compatible with standard purification methods, making it well-suited for iterative synthetic workflows in drug discovery.
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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-P280-P302+P352
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Lot numbers can be found on the outside label of a product: