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Structure of 3551-55-1
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2,4-Dimethoxypyrimidine serves as a key heterocyclic scaffold in medicinal chemistry, featuring two methoxy groups that enhance solubility and modulate electronic properties. This bench-stable compound integrates readily into kinase inhibitors and antiviral agents, offering predictable reactivity in nucleophilic substitution and cross-coupling transformations under standard conditions.
2,4-Dimethoxypyrimidine serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling efficient construction of heterocyclic scaffolds. Its two methoxy groups provide orthogonal reactivity for selective functionalization, while the pyrimidine core offers excellent stability and compatibility with standard coupling conditions. The compound facilitates direct substitution at C5 and subsequent derivatization, making it particularly valuable for accessing substituted pyrimidines via palladium-catalyzed cross-coupling or nucleophilic displacement reactions.
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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: