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Structure of 22813-32-7
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This imidazole-based carboxylic acid integrates a nitro-substituted heterocycle with a reactive acetic acid handle, enabling direct conjugation in bioconjugation workflows. The electron-deficient imidazolyl ring enhances reactivity in nucleophilic environments, while the bench-stable functionality simplifies handling under standard conditions.
2-(2-Nitro-1H-imidazol-1-yl)acetic acid serves as a versatile building block for bioactive heterocycles, enabling efficient access to imidazole-based scaffolds through standard functional group manipulations. The nitro group facilitates reduction and subsequent cyclization, while the carboxylic acid supports derivatization and purification via standard aqueous workups. Its bench-stable nature and compatibility with diverse reaction conditions make it suitable for medicinal chemistry campaigns and API intermediate synthesis.
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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: