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Structure of 4214-85-1
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2-Amino-6-methyl-5-nitro-3H-pyrimidin-4-one features a conjugated pyrimidinone core bearing a nitro group at C5 and a methyl substituent at C6, enhancing electron deficiency. This scaffold integrates readily into heterocyclic syntheses, offering utility in medicinal chemistry and materials science applications under standard conditions.
2-Amino-6-methyl-5-nitro-3H-pyrimidin-4-one serves as a versatile heterocyclic building block for medicinal chemistry and agrochemical research. Its amino, nitro, and carbonyl functionalities enable diverse transformations, including nucleophilic substitutions, reduction of the nitro group, and coupling reactions. The compound exhibits good bench stability and facilitates straightforward purification, making it suitable for iterative synthesis workflows in 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 : 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: