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Structure of 7153-13-1
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2-Amino-4,6-dichloro-5-methylpyrimidine serves as a key heterocyclic scaffold in medicinal chemistry, featuring a sterically accessible amino group and two chlorine substituents that enhance electrophilic reactivity. The methyl moiety improves solubility and metabolic stability, enabling efficient coupling in transition-metal-catalyzed transformations. This bench-stable compound facilitates rapid access to substituted pyrimidines under standard conditions.
2-Amino-4,6-dichloro-5-methylpyrimidine serves as a versatile building block in heterocyclic synthesis, enabling efficient access to substituted pyrimidines via nucleophilic substitution and coupling reactions. Its dichloro functionality provides orthogonal reactivity for sequential functionalization, while the amino and methyl groups offer enhanced solubility and stability under standard bench conditions. This compound facilitates the construction of pharmaceutically relevant scaffolds with predictable regioselectivity and high yields.
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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: