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Structure of 84332-06-9
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4-Methoxy-2-(methylthio)pyrimidine-5-carboxylic acid features a pyrimidine core functionalized with methoxy, methylthio, and carboxylic acid groups, enabling integration into bioactive scaffolds. The electron-rich heterocycle supports conjugation and metal coordination, while the carboxylic acid facilitates derivatization. This compound serves as a key intermediate in medicinal chemistry and agrochemical synthesis.
4-Methoxy-2-(methylthio)pyrimidine-5-carboxylic acid serves as a versatile building block in medicinal chemistry, enabling the synthesis of pyrimidine-based scaffolds through established coupling and functional group interconversions. Its carboxylic acid functionality facilitates amide bond formation, while the methoxy and methylthio groups provide orthogonal handles for selective derivatization. The compound exhibits good bench stability and is compatible with standard purification methods, supporting efficient integration into multi-step synthetic sequences for API development.
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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+H312+H332
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Precautionary Statements : P235-P261-P264-P270-P271-P273-P280-P302+P352-P304+P340-P330-P405-P501
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Lot numbers can be found on the outside label of a product: