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Structure of 4359-87-9
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2,4,6-Trichloro-5-nitropyrimidine serves as a key electrophilic heterocyclic scaffold for constructing advanced synthetic intermediates. The molecule features three chlorine substituents at high reactivity positions and a strongly electron-withdrawing nitro group at C5, enabling efficient coupling reactions under mild conditions. This combination delivers robust functionality in pharmaceutical and agrochemical synthesis.
2,4,6-Trichloro-5-nitropyrimidine serves as a versatile building block in heterocyclic synthesis, enabling efficient access to substituted pyrimidines via nucleophilic substitution. The trichloro and nitro groups provide orthogonal reactivity, facilitating sequential functionalization under mild conditions. Its bench-stable nature and compatibility with diverse coupling partners make it well-suited for medicinal chemistry campaigns and API intermediate 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-H319
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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: