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Structure of 1431412-19-9
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4-Methoxyfuro[3,2-d]pyrimidine-6-carboxylic acid features a fused heterocyclic core combining a furo[3,2-d]pyrimidine scaffold with a methoxy-substituted furan ring and a carboxylic acid at the C6 position. This configuration imparts enhanced solubility and stability under standard bench conditions, enabling direct incorporation into synthetic sequences for medicinal chemistry applications.
4-Methoxyfuro[3,2-d]pyrimidine-6-carboxylic acid serves as a versatile heterocyclic building block for medicinal chemistry and materials science applications. Its fused furanopyrimidine core provides enhanced metabolic stability and tunable solubility, while the carboxylic acid group enables direct derivatization via amide coupling or esterification. The methoxy substituent enhances electron density at the pyrimidine ring, facilitating electrophilic substitution and enabling access to diverse analogs. This compound exhibits excellent bench stability and compatibility with standard purification methods, making it well-suited for high-throughput synthesis and scale-up 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-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: