4-[(Furan-2-ylcarbonyl)amino]-3-methylbenzoic acid, with the CAS number 435288-00-9, is an organic compound characterized by its complex structure that includes a furan ring, an amine group, and a carboxylic acid functional group. This compound features a benzoic acid backbone substituted with a methyl group and a furan-2-ylcarbonylamino moiety, which contributes to its potential biological activity. The presence of the furan ring may impart unique electronic properties and reactivity, while the carboxylic acid group can participate in hydrogen bonding and ionic interactions, making it soluble in polar solvents. Its structural features suggest potential applications in pharmaceuticals or as a biochemical probe, particularly in studies involving enzyme inhibition or receptor binding. The compound's synthesis and characterization would typically involve standard organic chemistry techniques, including purification methods such as crystallization or chromatography. Overall, this compound exemplifies the intersection of heterocyclic chemistry and aromatic compounds, showcasing the diversity of organic molecules in chemical research.

4-[(furan-2-ylcarbonyl)amino]-3-methylbenzoic acid

435288-00-9: 4-[(Furan-2-ylcarbonyl)amino]-3-methylbenzoic acid, with the CAS number 435288-00-9, is an organic compound characterized by its complex structure that includes a furan ring, an amine group, and a carboxylic acid functional group. This compound features a benzoic acid backbone substituted with a methyl group and a furan-2-ylcarbonylamino moiety, which contributes to its potential biological activity. The presence of the furan ring may impart unique electronic properties and reactivity, while the carboxylic acid group can participate in hydrogen bonding and ionic interactions, making it soluble in polar solvents. Its structural features suggest potential applications in pharmaceuticals or as a biochemical probe, particularly in studies involving enzyme inhibition or receptor binding. The compound's synthesis and characterization would typically involve standard organic chemistry techniques, including purification methods such as crystallization or chromatography. Overall, this compound exemplifies the intersection of heterocyclic chemistry and aromatic compounds, showcasing the diversity of organic molecules in chemical research.

CAS 435288-00-9

4-[(furan-2-ylcarbonyl)amino]-3-methylbenzoic acid

4-(2-furoylamino)-3-methylbenzoic acid

Ref: IN-DA00DD2U

4-(2-furoylamino)-3-methylbenzoic acid

Ref: 10-F315596