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Structure of 5033-28-3
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4-Chloro-N-hydroxybenzimidamide delivers a reactive hydroxylamine moiety paired with a chlorinated benzimidazole scaffold, enabling efficient coupling in bioconjugation and medicinal chemistry applications. This bench-stable compound features enhanced solubility and selective reactivity under standard conditions.
4-Chloro-N-hydroxybenzimidamide serves as a versatile building block for heterocyclic synthesis, enabling efficient access to bioactive benzimidazole derivatives. Its N–OH functionality facilitates direct amidation and coupling reactions, while the chloro substituent supports palladium-catalyzed cross-coupling transformations. The compound exhibits good bench stability and is readily purified by recrystallization, making it suitable for iterative medicinal chemistry campaigns and API intermediate development.
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GHS Pictogram :
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GHS No : GHS06,GHS09
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Signal Word : Danger
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UN#: 2811
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Class : 6.1
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Packing Group : Ⅲ
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Hazard Statements : H301-H317-H400
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Precautionary Statements : P261-P264-P270-P272-P273-P280-P302+P352-P330-P363-P381-P501
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Lot numbers can be found on the outside label of a product: