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Structure of 93416-51-4
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2,4,6-Trichloropyrimidine-5-carboxylic acid features a highly electron-deficient pyrimidine core flanked by three chlorine substituents, enabling efficient coupling in nucleophilic aromatic substitution reactions. The carboxylic acid group provides a versatile handle for derivatization, facilitating incorporation into bioconjugates and pharmaceutical intermediates under mild conditions. This compound exhibits excellent stability and compatibility with diverse reaction environments.
2,4,6-Trichloropyrimidine-5-carboxylic acid serves as a versatile building block in heterocyclic synthesis, enabling efficient access to substituted pyrimidines via nucleophilic aromatic substitution. The trichloro pattern provides high reactivity at C2, C4, and C6 positions, while the carboxylic acid group facilitates derivatization and purification. Its bench stability and compatibility with standard coupling protocols make it a practical choice for medicinal chemistry 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-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: