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Structure of 50700-55-5
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1-Methyl-2-nitro-1H-imidazole-5-carboxylic acid features a fused heterocyclic core with complementary electron-withdrawing nitro and carboxylic acid groups, enabling direct functionalization in synthetic routes. The methyl substitution enhances solubility and stability under standard conditions. This compound serves as a key building block for bioactive imidazole derivatives in medicinal chemistry and materials science.
1-Methyl-2-nitro-1H-imidazole-5-carboxylic acid serves as a versatile building block in medicinal chemistry, enabling the construction of bioactive heterocycles through standard functional group manipulations. Its compatibility with diverse reaction conditions—particularly in amide coupling and nucleophilic substitution—facilitates rapid access to imidazole-based scaffolds. The molecule exhibits bench stability, ease of purification, and predictable reactivity, making it well-suited for high-throughput synthesis and process development workflows.
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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-P280-P302+P352
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Lot numbers can be found on the outside label of a product: