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Structure of 89581-88-4
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N-(2,4-Dichloropyrimidin-5-yl)acetamide features a pyrimidine core functionalized with two chlorine atoms at the 2- and 4-positions, enabling strong electron-withdrawing effects. The acetamide group provides a polar, hydrogen-bond-capable handle for coupling reactions. This structure integrates readily into pharmaceutical intermediates and agrochemical scaffolds, offering enhanced metabolic stability and targeted binding affinity in kinase inhibitors and DNA-targeting agents.
N-(2,4-Dichloropyrimidin-5-yl)acetamide serves as a versatile building block in medicinal chemistry, enabling efficient construction of heterocyclic scaffolds through nucleophilic substitution and coupling reactions. The dichloropyrimidine core exhibits high reactivity toward amines and thiols, facilitating rapid diversification. Bench-stable and readily purified by recrystallization, it functions reliably in standard synthetic workflows for 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 : H315-H319-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: