Oxazole, 4-methyl-2-phenyl- (CAS 877-39-4) is a heterocyclic organic compound characterized by a five-membered ring containing both nitrogen and oxygen atoms. The structure features a methyl group at the 4-position and a phenyl group at the 2-position of the oxazole ring, contributing to its unique chemical properties. This compound is typically a colorless to pale yellow liquid or solid, depending on its purity and specific conditions. It exhibits moderate solubility in organic solvents, which is common for many oxazole derivatives. The presence of the phenyl group enhances its aromatic character, potentially influencing its reactivity and interactions with other chemical species. Oxazole derivatives are known for their biological activity, making them of interest in medicinal chemistry and material science. Additionally, the compound may participate in various chemical reactions, such as electrophilic substitutions or nucleophilic attacks, due to the electron-rich nature of the oxazole ring. Overall, 4-methyl-2-phenyl-oxazole is a versatile compound with applications in various fields, including pharmaceuticals and agrochemicals.

Oxazole,4-methyl-2-phenyl-

877-39-4: Oxazole, 4-methyl-2-phenyl- (CAS 877-39-4) is a heterocyclic organic compound characterized by a five-membered ring containing both nitrogen and oxygen atoms. The structure features a methyl group at the 4-position and a phenyl group at the 2-position of the oxazole ring, contributing to its unique chemical properties. This compound is typically a colorless to pale yellow liquid or solid, depending on its purity and specific conditions. It exhibits moderate solubility in organic solvents, which is common for many oxazole derivatives. The presence of the phenyl group enhances its aromatic character, potentially influencing its reactivity and interactions with other chemical species. Oxazole derivatives are known for their biological activity, making them of interest in medicinal chemistry and material science. Additionally, the compound may participate in various chemical reactions, such as electrophilic substitutions or nucleophilic attacks, due to the electron-rich nature of the oxazole ring. Overall, 4-methyl-2-phenyl-oxazole is a versatile compound with applications in various fields, including pharmaceuticals and agrochemicals.

CAS 877-39-4

Oxazole,4-methyl-2-phenyl-

4-Methyl-2-phenyl-1,3-oxazole

Ref: 54-OR110144

4-methyl-2-phenyl-1,3-oxazole

Ref: 10-F518092