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Structure of 1920-66-7
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2-Chloro-5-nitropyrimidin-4-amine features a dual-functional pyrimidine core bearing a chlorine at C2 and a nitro group at C5, enabling selective coupling reactions. The amine handle at C4 facilitates conjugation in synthetic pathways. This electron-deficient scaffold supports efficient derivatization under mild conditions, offering high stability and compatibility with diverse reaction environments.
2-Chloro-5-nitropyrimidin-4-amine serves as a versatile building block in medicinal chemistry, enabling efficient construction of pyrimidine-based scaffolds. The chloro group facilitates nucleophilic substitution reactions, while the nitro and amine functionalities provide orthogonal handles for downstream functionalization. Its bench-stable nature and compatibility with standard coupling protocols make it well-suited for modular synthesis of heterocyclic compounds and API intermediates.
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GHS Pictogram :
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GHS No : GHS07,GHS08
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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-H334-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P284-P302+P352-P304+P340-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: