Methyl 2-phenyl-1,3-thiazole-5-carboxylate is an organic compound characterized by its thiazole ring, which is a five-membered heterocyclic structure containing sulfur and nitrogen. This compound features a carboxylate functional group, which contributes to its reactivity and solubility in polar solvents. The presence of the phenyl group enhances its aromatic characteristics and may influence its biological activity. Typically, compounds like this can exhibit various properties such as moderate to high melting points, depending on their molecular interactions and crystalline structure. Methyl 2-phenyl-1,3-thiazole-5-carboxylate may also display interesting pharmacological properties, making it a subject of interest in medicinal chemistry. Its synthesis often involves multi-step organic reactions, and it can be utilized in the development of pharmaceuticals, agrochemicals, or as a building block in organic synthesis. As with many thiazole derivatives, it may also show potential as a ligand in coordination chemistry or as a precursor in the synthesis of more complex molecules.

methyl 2-phenyl-1,3-thiazole-5-carboxylate

172678-68-1: Methyl 2-phenyl-1,3-thiazole-5-carboxylate is an organic compound characterized by its thiazole ring, which is a five-membered heterocyclic structure containing sulfur and nitrogen. This compound features a carboxylate functional group, which contributes to its reactivity and solubility in polar solvents. The presence of the phenyl group enhances its aromatic characteristics and may influence its biological activity. Typically, compounds like this can exhibit various properties such as moderate to high melting points, depending on their molecular interactions and crystalline structure. Methyl 2-phenyl-1,3-thiazole-5-carboxylate may also display interesting pharmacological properties, making it a subject of interest in medicinal chemistry. Its synthesis often involves multi-step organic reactions, and it can be utilized in the development of pharmaceuticals, agrochemicals, or as a building block in organic synthesis. As with many thiazole derivatives, it may also show potential as a ligand in coordination chemistry or as a precursor in the synthesis of more complex molecules.

CAS 172678-68-1

methyl 2-phenyl-1,3-thiazole-5-carboxylate

Methyl 2-phenylthiazole-5-carboxylate

Ref: IN-DA00AMQ8

Methyl 2-phenylthiazole-5-carboxylate

Ref: 10-F236905

Methyl 2-phenylthiazole-5-carboxylate

Ref: 3D-XGA67868