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Structure of 72411-89-3
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4-Methoxypyrimidine-5-carboxylic acid features a pyrimidine core bearing a methoxy group at the 4-position and a carboxylic acid at the 5-position, enabling direct conjugation or derivatization. The electron-withdrawing carboxyl moiety enhances reactivity in coupling processes, while the methoxy substituent provides steric and electronic modulation. This scaffold integrates readily into bioactive molecules and functional materials under standard conditions.
4-Methoxypyrimidine-5-carboxylic acid serves as a versatile building block for heterocyclic synthesis, enabling efficient access to pyrimidine-based scaffolds relevant in medicinal chemistry. Its dual functionality—electron-withdrawing carboxylic acid and electron-donating methoxy group—facilitates regioselective functionalization and supports diverse coupling reactions. The compound exhibits good bench stability and is compatible with standard purification methods, making it well-suited for iterative synthetic workflows in 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-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: