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


Chemical Name: 5-(1-methylpyrrol-2-yl)-1,2-oxazole-3-carboxylic acid
CAS Number: 1326814-81-6
Product Number: AG0010ZA(AGN-PC-0I7YUW)
Synonyms:
MDL No: MFCD19706940
Molecular Formula: C9H8N2O3
Molecular Weight: 192.1714

Identification/Properties


Safety Information


GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P280-P301+P312-P302+P352-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum


Other Analytical Data


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Chemical Structure



5-(1-Methyl-1H-pyrrol-2-yl)isoxazole-3-carboxylic acid is a versatile compound utilized in chemical synthesis as a key building block for the creation of novel organic molecules. With its unique structure and functional groups, this compound serves as a valuable precursor in the development of pharmaceuticals, agrochemicals, and materials science.In chemical synthesis, 5-(1-Methyl-1H-pyrrol-2-yl)isoxazole-3-carboxylic acid can participate in various reactions such as cross-coupling, esterification, amidation, and cyclization. Its reactive carboxylic acid group allows for selective functionalization, enabling the introduction of different substituents to tailor the properties of the final product. Additionally, the isoxazole ring provides a scaffold for further diversification through modification of its nitrogen and carbon atoms.Furthermore, the incorporation of the pyrrole moiety in the molecule imparts unique electronic properties, making 5-(1-Methyl-1H-pyrrol-2-yl)isoxazole-3-carboxylic acid an attractive candidate for the design of bioactive compounds and materials with specific functionalities. Its compatibility with a wide range of synthetic methods and its structural features make it a valuable tool for organic chemists seeking to access structurally complex compounds with desired properties.