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Structure of 271-70-5
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7H-Pyrrolo[2,3-d]pyrimidine serves as a core heterocyclic scaffold in medicinal chemistry, offering a rigid, electron-rich framework ideal for kinase inhibitor design. This planar, nitrogen-rich system integrates seamlessly into bioactive molecules, enhancing target binding affinity and metabolic stability through favorable π-stacking interactions.
7H-Pyrrolo[2,3-d]pyrimidine serves as a privileged heterocyclic scaffold in medicinal chemistry, enabling the construction of biologically active compounds through well-established functionalization at the 2-, 4-, and 7-positions. Its inherent stability and compatibility with standard coupling reactions facilitate efficient synthesis of kinase inhibitors and nucleoside analogs. The core functions as a versatile building block for drug discovery campaigns requiring planar, electron-rich aromatic systems with tunable hydrogen-bonding capacity.
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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: