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Structure of 1192711-37-7
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This pyrimidine derivative features a cyclopropylamino group and a carboxylic acid at the 4- and 5-positions, respectively, enabling direct integration into bioactive scaffolds. The electron-deficient pyrimidine core supports efficient coupling reactions under standard conditions, while the carboxylic acid facilitates conjugation without requiring activation.
2-Chloro-4-(cyclopropylamino)pyrimidine-5-carboxylic acid serves as a versatile building block in the synthesis of pyrimidine-based heterocycles, enabling efficient access to medicinally relevant scaffolds. Its functional group array—comprising a chloro substituent, cyclopropylamino handle, and carboxylic acid—facilitates diverse downstream transformations including nucleophilic substitution, amide coupling, and cyclization reactions. The compound exhibits bench stability and is readily purified by standard techniques, supporting its utility in high-throughput medicinal chemistry campaigns 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
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Precautionary Statements : P264-P270-P330-P501
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Lot numbers can be found on the outside label of a product: