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Structure of 38214-45-8
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6-Methoxypyrimidine-4-carboxylic acid features a pyrimidine core functionalized with methoxy and carboxylic acid groups at positions 6 and 4, respectively. This configuration imparts enhanced solubility and stability under standard conditions. The electron-withdrawing nature of the carboxylate facilitates coupling reactions, while the methoxy group provides steric and electronic modulation. The molecule serves as a key building block in the synthesis of bioactive heterocycles and pharmaceutical intermediates.
6-Methoxypyrimidine-4-carboxylic acid serves as a versatile building block for heterocyclic synthesis, enabling efficient access to pyrimidine-based scaffolds through standard coupling and functionalization protocols. Its dual functionality—carboxylic acid and methoxy groups—supports diverse transformations, including amidation, esterification, and metal-catalyzed cross-couplings. The compound exhibits good bench stability and facilitates straightforward purification, making it well-suited for medicinal chemistry campaigns and process development in API synthesis.
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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: