1-(4-Trifluoromethyl-benzyl)-piperidine-3-carboxylic acid hydrochloride is a chemical compound characterized by its piperidine core, which is a six-membered nitrogen-containing ring. The presence of a trifluoromethyl group on the benzyl moiety significantly influences its chemical properties, enhancing lipophilicity and potentially affecting biological activity. This compound is typically a white to off-white solid and is soluble in polar solvents, which is common for carboxylic acid derivatives. The hydrochloride salt form indicates that it is a protonated species, which can enhance its stability and solubility in aqueous environments. Its structure suggests potential applications in medicinal chemistry, particularly in the development of pharmaceuticals, due to the piperidine ring's role in various biological activities. The trifluoromethyl group may also contribute to the compound's ability to interact with biological targets, making it of interest in drug design and development. As with many chemical substances, handling should be done with care, following appropriate safety protocols due to potential toxicity and reactivity.

1-(4-TRIFLUOROMETHYL-BENZYL)-PIPERIDINE-3-CARBOXYLIC ACID HYDROCHLORIDE

896046-07-4: 1-(4-Trifluoromethyl-benzyl)-piperidine-3-carboxylic acid hydrochloride is a chemical compound characterized by its piperidine core, which is a six-membered nitrogen-containing ring. The presence of a trifluoromethyl group on the benzyl moiety significantly influences its chemical properties, enhancing lipophilicity and potentially affecting biological activity. This compound is typically a white to off-white solid and is soluble in polar solvents, which is common for carboxylic acid derivatives. The hydrochloride salt form indicates that it is a protonated species, which can enhance its stability and solubility in aqueous environments. Its structure suggests potential applications in medicinal chemistry, particularly in the development of pharmaceuticals, due to the piperidine ring's role in various biological activities. The trifluoromethyl group may also contribute to the compound's ability to interact with biological targets, making it of interest in drug design and development. As with many chemical substances, handling should be done with care, following appropriate safety protocols due to potential toxicity and reactivity.

CAS 896046-07-4

1-(4-TRIFLUOROMETHYL-BENZYL)-PIPERIDINE-3-CARBOXYLIC ACID HYDROCHLORIDE

1-(4-TRIFLUOROMETHYL-BENZYL)-PIPERIDINE-3-CARBOXYLIC ACID HYDROCHLORIDE

Ref: IN-DA003XJ4