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Structure of 698-16-8
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N-Hydroxybenzimidoyl chloride delivers a reactive acylating moiety for direct incorporation into amine-functionalized substrates. This bench-stable reagent features a hydroxyl-activated imidoyl chloride group, enabling efficient formation of benzimidoyl esters under mild conditions. Ideal for peptide derivatization and bioconjugation workflows requiring selective C–O bond activation.
N-Hydroxybenzimidoyl chloride serves as a versatile acylating agent for the synthesis of benzimidazole derivatives and oxime esters. Its reactivity enables efficient conversion of carboxylic acids to acyl chlorides under mild conditions, with high functional group tolerance and excellent bench stability. The compound facilitates straightforward access to heterocyclic scaffolds relevant in medicinal chemistry and acts as a key intermediate in the construction of bioactive molecules through selective amide and ester bond formation.
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GHS Pictogram :
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GHS No : GHS02,GHS06
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Signal Word : Danger
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UN#: 2926
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Class : 4.1,6.1
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Packing Group : Ⅲ
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Hazard Statements : H228-H301
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Precautionary Statements : P210-P240-P264-P270-P280-P330-P370+P378-P405-P501
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Lot numbers can be found on the outside label of a product: