CAS 1024364-57-5

5H-Thiazolo[3,2-a]pyrimidine-6-carboxylic acid, 3,7-dimethyl-5-phenyl-, ethyl ester

Description:

5H-Thiazolo[3,2-a]pyrimidine-6-carboxylic acid, 3,7-dimethyl-5-phenyl-, ethyl ester is a chemical compound characterized by its unique thiazolo and pyrimidine ring structures, which contribute to its potential biological activity. This compound features a carboxylic acid functional group, which is esterified with an ethyl group, enhancing its solubility and reactivity. The presence of methyl and phenyl substituents on the pyrimidine ring may influence its pharmacological properties, potentially affecting interactions with biological targets. The thiazole moiety adds to the compound's heterocyclic nature, which is often associated with diverse biological activities, including antimicrobial and anticancer properties. The compound's molecular structure suggests it may participate in various chemical reactions, making it of interest in medicinal chemistry and drug development. As with many heterocyclic compounds, its synthesis and characterization would involve standard organic chemistry techniques, and its biological evaluation would require rigorous testing to ascertain its efficacy and safety profiles.

Formula: C₁₇H₁₈N₂O₂S

Synonyms:

• Tyrosinase-IN-20
• 5H-Thiazolo[3,2-a]pyrimidine-6-carboxylic acid, 3,7-dimethyl-5-phenyl-, ethyl ester

Tyrosinase-IN-20

CAS: 1024364-57-5

Tyrosinase-IN-20 (compound 6a) acts as a potent Tyrosinase inhibitor, demonstrating an IC 50 value of 28.50 μM [1].

Formula: C₁₇H₁₈N₂O₂S

Color and Shape: Solid

Molecular weight: 314.4

Ref: TM-T87588