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Structure of 4319-93-1
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4,6-Dimethoxypyrimidine-5-carboxylic acid features a pyrimidine core functionalized with two methoxy groups and a carboxylic acid at the 5-position, offering enhanced solubility and stability under standard conditions. This scaffold serves as a key building block in medicinal chemistry, enabling efficient incorporation into bioactive molecules through coupling reactions.
4,6-Dimethoxypyrimidine-5-carboxylic acid serves as a versatile building block in medicinal chemistry, enabling the synthesis of pyrimidine-based scaffolds through established coupling and cyclization protocols. Its ortho-dicarbonyl motif facilitates efficient functionalization and offers enhanced bench stability compared to analogous intermediates. The molecule functions effectively in amide bond formation and transition-metal-catalyzed cross-coupling reactions, supporting scalable access to heterocyclic compounds with defined regiochemistry.
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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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: