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Structure of 914208-17-6
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2-(Methylsulfonyl)pyrimidine-5-carboxylic acid features a pyrimidine core functionalized with both a methylsulfonyl group and a carboxylic acid at the 2- and 5-positions, respectively. This dual functionality enables integration into diverse synthetic scaffolds, particularly in medicinal chemistry and materials science. The molecule exhibits enhanced solubility and stability under standard conditions, facilitating straightforward handling in reaction workflows.
2-(Methylsulfonyl)pyrimidine-5-carboxylic acid serves as a versatile building block in medicinal chemistry, enabling the synthesis of heterocyclic scaffolds through standard coupling and functionalization reactions. The carboxylic acid group facilitates amide bond formation and derivatization, while the methylsulfonyl moiety provides metabolic stability and enhanced solubility. Bench-stable and compatible with common protecting group strategies, it functions effectively in multi-step syntheses targeting kinase inhibitors and other bioactive molecules.
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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-H335-H319
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Precautionary Statements : P260-P264-P270-P271-P280-P301+P310-P302+P352-P304+P340-P305+P351+P338-P312-P330-P332+P313-P337+P313-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: