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Structure of 2604-39-9
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2-Chloro-5-nitropyridin-4-amine features a pyridine core functionalized with chlorine, nitro, and amino groups at positions 2, 5, and 4, respectively. This electron-deficient heterocycle integrates readily into cross-coupling reactions and serves as a key intermediate in the synthesis of advanced pharmaceuticals and agrochemicals.
2-Chloro-5-nitropyridin-4-amine serves as a versatile building block in medicinal chemistry, enabling efficient construction of pyridine-based heterocycles. Its orthogonally reactive chlorine and nitro groups facilitate sequential functionalization via nucleophilic substitution and reduction, respectively. The molecule exhibits good bench stability and compatibility with standard coupling reactions, making it well-suited for the synthesis of advanced intermediates 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: