The chemical substance known as ((4R,5R)-5-(4-Iodophenyl)-2-Phenyl-4,5-Dihydrooxazol-4-Yl)Methanol, with the CAS number 927689-68-7, is characterized by its complex molecular structure, which includes an oxazole ring and a phenyl group substituted with an iodine atom. This compound exhibits chirality due to the presence of stereocenters, specifically at the 4 and 5 positions of the oxazole ring, which can influence its biological activity and interactions. The presence of the hydroxymethyl group contributes to its potential solubility in polar solvents and may enhance its reactivity in various chemical reactions. Additionally, the iodine substituent can impart unique electronic properties, making it a candidate for applications in medicinal chemistry and material science. Its specific stereochemistry and functional groups suggest potential uses in drug development, particularly in targeting specific biological pathways or receptors. Overall, this compound's unique structural features make it a subject of interest in both synthetic and applied chemistry.

((4R,5R)-5-(4-Iodophenyl)-2-Phenyl-4,5-Dihydrooxazol-4-Yl)Methanol

927689-68-7: The chemical substance known as ((4R,5R)-5-(4-Iodophenyl)-2-Phenyl-4,5-Dihydrooxazol-4-Yl)Methanol, with the CAS number 927689-68-7, is characterized by its complex molecular structure, which includes an oxazole ring and a phenyl group substituted with an iodine atom. This compound exhibits chirality due to the presence of stereocenters, specifically at the 4 and 5 positions of the oxazole ring, which can influence its biological activity and interactions. The presence of the hydroxymethyl group contributes to its potential solubility in polar solvents and may enhance its reactivity in various chemical reactions. Additionally, the iodine substituent can impart unique electronic properties, making it a candidate for applications in medicinal chemistry and material science. Its specific stereochemistry and functional groups suggest potential uses in drug development, particularly in targeting specific biological pathways or receptors. Overall, this compound's unique structural features make it a subject of interest in both synthetic and applied chemistry.

CAS 927689-68-7

((4R,5R)-5-(4-Iodophenyl)-2-Phenyl-4,5-Dihydrooxazol-4-Yl)Methanol

((4R,5R)-5-(4-Iodophenyl)-2-phenyl-4,5-dihydrooxazol-4-yl)methanol

Ref: IN-DA0060VA

((4R,5R)-5-(4-Iodophenyl)-2-phenyl-4,5-dihydrooxazol-4-yl)methanol

Ref: 10-F213742