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Structure of 1260088-59-2
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This pyrano[3,2-d]pyrimidine scaffold integrates electron-deficient halogen substituents at the 2,4-positions, enhancing its reactivity in cross-coupling transformations. The fused dihydro-pyran ring imparts conformational rigidity and improved solubility in polar aprotic solvents, enabling efficient incorporation into complex heterocyclic architectures under standard conditions.
2,4-Dichloro-7,8-dihydro-6H-pyrano[3,2-d]pyrimidine serves as a versatile building block in heterocyclic synthesis, enabling efficient access to pyrano[3,2-d]pyrimidine scaffolds prevalent in medicinal chemistry. Its dichloro substitution pattern facilitates downstream functionalization via nucleophilic displacement, while the dihydro-pyrano core exhibits bench stability and compatibility with standard reaction conditions. The compound functions effectively in Pd-catalyzed cross-coupling and cycloaddition protocols, supporting scalable route development for advanced intermediates.
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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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: