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Structure of 491-11-2
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3-Chloro-4-nitrophenol features a chlorinated aromatic ring paired with a nitro group in the para position relative to the hydroxyl, delivering enhanced electron-withdrawing character. This combination enables selective reactivity in nucleophilic substitution and coupling reactions. The compound exhibits bench-stable handling properties and integrates readily into synthetic pathways requiring activated aryl intermediates.
3-Chloro-4-nitrophenol serves as a versatile building block in synthetic organic chemistry, enabling the construction of heterocyclic scaffolds and functionalized aryl intermediates. Its ortho-chloro and para-nitro substituents provide complementary reactivity for nucleophilic substitution, coupling reactions, and reduction sequences. The compound exhibits good bench stability and facilitates straightforward purification, making it well-suited for multi-step synthesis in medicinal chemistry and agrochemical development.
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GHS No : GHS05,GHS07,GHS09
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Signal Word : Danger
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UN#: 3077
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Class : 9
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Packing Group : Ⅲ
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Hazard Statements : H302-H315-H317-H318-H410
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Precautionary Statements : P261-P264-P270-P272-P273-P280-P302+P352-P330-P362+P364-P391-P501
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Lot numbers can be found on the outside label of a product: