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Structure of 14916-64-4
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2-Nitropyridin-4-amine delivers a strategically positioned nitro group and amine functionality on a pyridine scaffold, enabling direct integration into cross-coupling reactions and metal-ligand coordination. This electron-deficient heterocycle serves as a key intermediate in medicinal chemistry, facilitating the construction of bioactive molecules through selective functionalization.
2-Nitropyridin-4-amine serves as a versatile building block in medicinal chemistry, enabling efficient construction of nitrogen-containing heterocycles. Its dual functionality—nitro group at C2 and amino group at C4—supports sequential transformations via selective reduction, coupling, or electrophilic substitution. The compound exhibits good bench stability and facilitates straightforward purification, making it well-suited for multi-step synthesis workflows targeting API scaffolds.
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GHS Pictogram :
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GHS No : GHS05
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Signal Word : Danger
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UN#: 3261
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Class : 8
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Packing Group : Ⅲ
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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: