Piperidin-4-yl(thiophen-2-yl)methanone hydrochloride is a chemical compound characterized by its piperidine ring, which is a six-membered saturated nitrogen-containing heterocycle, and a thiophene moiety, which is a five-membered aromatic ring containing sulfur. This compound typically appears as a white to off-white crystalline solid and is soluble in polar solvents such as water and alcohols, owing to the presence of the hydrochloride salt form. The presence of both the piperidine and thiophene groups suggests potential biological activity, making it of interest in medicinal chemistry, particularly in the development of pharmaceuticals. The hydrochloride salt form enhances its stability and solubility, which is advantageous for various applications, including drug formulation. As with many organic compounds, it is essential to handle this substance with care, following appropriate safety protocols, as it may exhibit specific toxicity or reactivity profiles. Its unique structural features may contribute to its interaction with biological targets, warranting further investigation in drug discovery contexts.

piperidin-4-yl(thiophen-2-yl)methanone hydrochloride

219540-76-8: Piperidin-4-yl(thiophen-2-yl)methanone hydrochloride is a chemical compound characterized by its piperidine ring, which is a six-membered saturated nitrogen-containing heterocycle, and a thiophene moiety, which is a five-membered aromatic ring containing sulfur. This compound typically appears as a white to off-white crystalline solid and is soluble in polar solvents such as water and alcohols, owing to the presence of the hydrochloride salt form. The presence of both the piperidine and thiophene groups suggests potential biological activity, making it of interest in medicinal chemistry, particularly in the development of pharmaceuticals. The hydrochloride salt form enhances its stability and solubility, which is advantageous for various applications, including drug formulation. As with many organic compounds, it is essential to handle this substance with care, following appropriate safety protocols, as it may exhibit specific toxicity or reactivity profiles. Its unique structural features may contribute to its interaction with biological targets, warranting further investigation in drug discovery contexts.

CAS 219540-76-8

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