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Structure of 2227-98-7
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4-Aminopyrrolo[3,2-d]pyrimidine delivers a planar, electron-rich heterocyclic scaffold ideal for constructing kinase inhibitors and bioactive small molecules. This nitrogen-rich core integrates readily into pharmaceutical intermediates, offering enhanced solubility and predictable reactivity under standard conditions.
4-Aminopyrrolo[3,2-d]pyrimidine serves as a versatile heterocyclic scaffold in medicinal chemistry, enabling efficient construction of purine analogs and kinase inhibitor candidates. Its amino group facilitates direct functionalization and metal-catalyzed coupling reactions, while the fused bicyclic framework offers enhanced metabolic stability. The compound exhibits good bench stability and compatibility with standard purification methods, making it well-suited for iterative synthesis 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-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: