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Structure of 1260665-09-5
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This bench-stable triazole derivative features a tert-butyl group that enhances solubility and steric protection, while the carboxylic acid moiety enables direct conjugation or derivatization. The electron-deficient triazole ring facilitates efficient copper-catalyzed azide-alkyne cycloaddition (CuAAC) reactions, making it ideal for bioconjugation and materials functionalization under mild conditions.
1-(tert-Butyl)-1H-1,2,3-triazole-4-carboxylic acid serves as a stable, bench-ready building block for bioactive heterocycles and peptide conjugates. The triazole ring enables reliable copper-catalyzed azide-alkyne cycloaddition (CuAAC), while the carboxylic acid facilitates amide coupling and derivatization. Its tert-butyl group enhances solubility and simplifies purification, making it ideal for modular synthesis in medicinal chemistry and chemical biology workflows.
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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: