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Structure of 878742-59-7
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2-(Trifluoromethyl)pyrimidine-4-carboxylic acid features a trifluoromethyl group at the 2-position and a carboxylic acid at the 4-position on a pyrimidine scaffold, delivering enhanced electron-withdrawing character and metabolic stability. This combination enables robust integration into bioactive molecules, particularly in kinase inhibitors and pharmaceutical scaffolds requiring high lipophilicity and targeted reactivity. The compound exhibits excellent bench stability and solubility under standard conditions, facilitating use in synthetic workflows.
2-(Trifluoromethyl)pyrimidine-4-carboxylic acid serves as a versatile building block in medicinal chemistry, enabling the synthesis of bioactive heterocycles through standard coupling and functionalization reactions. Its trifluoromethyl group enhances metabolic stability and lipophilicity, while the carboxylic acid facilitates direct derivatization or incorporation into peptide-like scaffolds. The molecule exhibits good bench stability and compatibility with common reaction conditions, making it well-suited for iterative synthesis campaigns targeting kinase inhibitors and other pharmaceutical candidates.
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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: