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Structure of 13106-85-9
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2,4,6-Trimethoxypyrimidine features three methoxy groups positioned at key electronic sites, enhancing its reactivity in nucleophilic substitution and transition metal-catalyzed coupling reactions. This bench-stable heterocycle serves as a robust scaffold for pharmaceutical intermediates and functional materials, offering predictable regioselectivity and compatibility with diverse synthetic transformations under standard conditions.
2,4,6-Trimethoxypyrimidine serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling efficient construction of pyrimidine-based scaffolds. Its three methoxy groups offer orthogonal reactivity for selective functionalization, while the core heterocycle exhibits excellent bench stability and compatibility with standard coupling conditions. The compound facilitates rapid diversification in lead optimization campaigns through reliable nucleophilic substitution and transition-metal-catalyzed transformations.
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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 : H315-H319-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362-P405-P501
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Lot numbers can be found on the outside label of a product: