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Structure of 1260088-72-9
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This furo[3,4-d]pyrimidine scaffold features two chlorine substituents at the 2 and 4 positions and two methyl groups flanking the central ring junction, delivering a sterically congested, electron-deficient core ideal for coupling reactions in medicinal chemistry and materials synthesis.
2,4-Dichloro-7,7-dimethyl-5H-furo[3,4-d]pyrimidine serves as a versatile building block in heterocyclic synthesis, enabling efficient access to fused pyrimidine scaffolds via nucleophilic substitution. Its dichloro functionality offers predictable reactivity at C2 and C4 positions, facilitating coupling with amines, alcohols, and thiols under mild conditions. The 7,7-dimethyl substitution enhances bench stability and simplifies purification. This compound functions as a key intermediate in the construction of biologically relevant frameworks, particularly in medicinal chemistry campaigns targeting kinase inhibitors and antiviral agents.
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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: