4-(5-Methylthiophen-2-yl)-1,3-thiazol-2-amine is an organic compound characterized by its unique structural features, which include a thiazole ring and a thiophene moiety. The thiazole ring contributes to its potential biological activity, often associated with compounds that exhibit antimicrobial or antifungal properties. The presence of the methylthio group enhances its lipophilicity, which can influence its solubility and permeability in biological systems. This compound is typically a solid at room temperature and may exhibit moderate stability under standard conditions. Its molecular structure suggests potential applications in pharmaceuticals, particularly in drug development, where thiazole derivatives are known for their diverse biological activities. Additionally, the compound's reactivity can be influenced by the functional groups present, making it a candidate for further chemical modifications. Safety and handling precautions should be observed, as with many organic compounds, due to potential toxicity or reactivity. Overall, 4-(5-methylthiophen-2-yl)-1,3-thiazol-2-amine represents a class of compounds with significant interest in medicinal chemistry.

4-(5-methylthiophen-2-yl)-1,3-thiazol-2-amine

383129-75-7: 4-(5-Methylthiophen-2-yl)-1,3-thiazol-2-amine is an organic compound characterized by its unique structural features, which include a thiazole ring and a thiophene moiety. The thiazole ring contributes to its potential biological activity, often associated with compounds that exhibit antimicrobial or antifungal properties. The presence of the methylthio group enhances its lipophilicity, which can influence its solubility and permeability in biological systems. This compound is typically a solid at room temperature and may exhibit moderate stability under standard conditions. Its molecular structure suggests potential applications in pharmaceuticals, particularly in drug development, where thiazole derivatives are known for their diverse biological activities. Additionally, the compound's reactivity can be influenced by the functional groups present, making it a candidate for further chemical modifications. Safety and handling precautions should be observed, as with many organic compounds, due to potential toxicity or reactivity. Overall, 4-(5-methylthiophen-2-yl)-1,3-thiazol-2-amine represents a class of compounds with significant interest in medicinal chemistry.

CAS 383129-75-7

4-(5-methylthiophen-2-yl)-1,3-thiazol-2-amine

4-(5-Methyl-thiophen-2-yl)-thiazol-2-ylamine

Ref: IN-DA00C606

4-(5-Methylthiophen-2-yl)thiazol-2-ylamine

Ref: 10-F014149

4-(5-Methyl-thiophen-2-yl)-thiazol-2-ylamine

Ref: 3D-IQA12975