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Structure of 93366-88-2
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7H-Pyrrolo[2,3-d]pyrimidin-2-amine features a fused heterocyclic core with a primary amine at the 2-position, offering a rigid, electron-rich scaffold ideal for kinase inhibitor design. This platform integrates seamlessly into medicinal chemistry campaigns requiring planar, hydrogen-bond-donating motifs with enhanced metabolic stability and favorable binding geometry in ATP-pocket environments.
7H-Pyrrolo[2,3-d]pyrimidin-2-amine serves as a versatile heterocyclic building block for medicinal chemistry and catalytic synthesis. Its fused bicyclic structure provides enhanced stability and predictable reactivity, enabling efficient functionalization at multiple positions. The amine group facilitates direct coupling reactions and derivatization, while the core scaffold exhibits favorable solubility and purification characteristics. Functions reliably in standard synthetic workflows for kinase inhibitor development and nucleoside analog construction.
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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: