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Structure of 5270-94-0
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4,6-Dimethoxypyrimidine serves as a key heterocyclic scaffold in medicinal chemistry, offering enhanced solubility and metabolic stability. The ortho-dimethoxy substitution pattern enables selective functionalization at C5, facilitating the synthesis of advanced intermediates for kinase inhibitors and antiviral agents. This bench-stable compound integrates readily into multistep sequences under mild conditions.
4,6-Dimethoxypyrimidine serves as a versatile building block in medicinal chemistry and synthetic organic chemistry, enabling efficient construction of heterocyclic scaffolds. Its ortho-dimethoxy substitution pattern enhances reactivity in nucleophilic displacement and transition-metal-catalyzed coupling reactions. The compound exhibits excellent bench stability, facilitates straightforward purification, and demonstrates broad functional group tolerance, making it ideal for iterative synthesis workflows and API development.
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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: