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Structure of 536755-29-0
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This imidazolium carboxylate features a proton-deficient C2 position, enabling direct functionalization in synthetic transformations. The dimethyl substitution enhances solubility in polar solvents while maintaining thermal stability under standard reaction conditions. This scaffold serves as a robust building block for ionic liquid design and catalytic systems requiring localized negative charge density.
1,3-Dimethylimidazolium-2-carboxylate serves as a versatile building block in the synthesis of functionalized imidazoles and heterocyclic scaffolds. Its carboxylate functionality enables direct amidation, esterification, or metal coordination, while the imidazolium core offers stability and compatibility with common organic transformations. The compound facilitates efficient access to biologically relevant motifs and is well-suited for scale-up due to its bench-stable nature and straightforward purification.
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GHS Pictogram :
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GHS No : GHS05
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Signal Word : Danger
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UN#: 3261
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Class : 8
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Packing Group : Ⅲ
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Hazard Statements : H318
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Precautionary Statements : P260-P264-P280-P301+P330+P331-P303+P361+P353-P304+P340-P305+P351+P338-P363-P405-P501
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Lot numbers can be found on the outside label of a product: