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Structure of 2137975-63-2
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4-Chloro-3-hydroxy-5-nitrobenzamide features a trifunctional aromatic core with chlorine, hydroxyl, and nitro groups positioned for orthogonal reactivity. This electron-deficient scaffold enables direct coupling in late-stage functionalization and serves as a key intermediate in the synthesis of bioactive heterocycles under mild conditions.
4-Chloro-3-hydroxy-5-nitrobenzamide serves as a versatile building block in medicinal chemistry, enabling the synthesis of heterocyclic scaffolds via cyclization or nucleophilic substitution. The ortho-chloro and nitro groups facilitate downstream functionalization, while the phenolic hydroxyl offers direct derivatization potential. Its bench-stable nature and compatibility with standard coupling reactions make it suitable for multi-step synthesis workflows in API development.
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GHS Pictogram :
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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: