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Structure of 1780-32-1
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2,4-Dichloro-5,6-dimethylpyrimidine serves as a pivotal building block in heterocyclic synthesis, featuring two chlorine atoms at electron-deficient positions and methyl groups that enhance regioselectivity. This bench-stable scaffold integrates readily into pharmaceutical intermediates and agrochemical frameworks, offering predictable reactivity under standard conditions.
2,4-Dichloro-5,6-dimethylpyrimidine serves as a versatile building block in medicinal chemistry and agrochemical synthesis. Its electron-deficient pyrimidine core enables nucleophilic substitution at C2 or C4 positions, facilitating the construction of diverse heterocyclic scaffolds. The methyl groups enhance metabolic stability and modulate electronic properties, while the dichloro substitution pattern provides orthogonal reactivity for sequential functionalization. This compound exhibits good bench stability and is compatible with standard coupling protocols, making it a practical choice for parallel synthesis campaigns and process 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: