5-(Furan-2-yl)-1,2-oxazole-3-carboxylic acid is an organic compound characterized by its unique structure, which includes a furan ring and an oxazole moiety. The presence of the furan ring contributes to its aromatic properties, while the oxazole provides heterocyclic characteristics. This compound typically exhibits moderate solubility in polar solvents due to the carboxylic acid functional group, which can engage in hydrogen bonding. It may display biological activity, making it of interest in medicinal chemistry and drug development. The carboxylic acid group can participate in various chemical reactions, such as esterification and amidation, allowing for further functionalization. Additionally, the compound's structure suggests potential applications in materials science and organic synthesis. Its CAS number, 98434-06-1, allows for easy identification in chemical databases, facilitating research and development efforts. Overall, 5-(furan-2-yl)-1,2-oxazole-3-carboxylic acid is a versatile compound with potential applications across various fields of chemistry.

5-(furan-2-yl)-1,2-oxazole-3-carboxylic acid

98434-06-1: 3-Isoxazolecarboxylic acid, 5-(2-furanyl)-, 5-(2-Furyl)-1,2-oxazole-3-carboxylic acid, 5-(2-Furyl)Isoxazole-3-Carboxylic Acid

5-(2-Furyl)isoxazole-3-carboxylic acid

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CAS 98434-06-1: 5-(furan-2-yl)-1,2-oxazole-3-carboxylic acid

5-(2-Furyl)isoxazole-3-carboxylic acid

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5-(2-Furyl)isoxazole-3-carboxylic acid

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5-Furan-2-yl-isoxazole-3-carboxylic acid

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5-(Furan-2-yl)isoxazole-3-carboxylic acid

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