1-[(2,4-Dichlorophenyl)methyl]-2-piperidinecarboxylic acid is a chemical compound characterized by its piperidine core, which is a six-membered nitrogen-containing ring. The presence of a 2,4-dichlorophenyl group indicates that the compound has two chlorine substituents on the phenyl ring, contributing to its potential biological activity and lipophilicity. This compound is likely to exhibit properties typical of carboxylic acids, such as the ability to form hydrogen bonds and participate in acid-base reactions. Its structure suggests potential applications in medicinal chemistry, particularly in the development of pharmaceuticals, due to the piperidine moiety, which is often found in various bioactive compounds. The compound's molecular weight, solubility, and stability would depend on the specific functional groups and their interactions. Additionally, the presence of chlorine atoms may influence its reactivity and environmental behavior. As with many synthetic organic compounds, safety and handling precautions are essential, given the potential toxicity associated with chlorinated aromatic compounds.

1-[(2,4-DICHLOROPHENYL)METHYL]-2-PIPERIDINECARBOXYLIC ACID

1042766-55-1: 1-[(2,4-Dichlorophenyl)methyl]-2-piperidinecarboxylic acid is a chemical compound characterized by its piperidine core, which is a six-membered nitrogen-containing ring. The presence of a 2,4-dichlorophenyl group indicates that the compound has two chlorine substituents on the phenyl ring, contributing to its potential biological activity and lipophilicity. This compound is likely to exhibit properties typical of carboxylic acids, such as the ability to form hydrogen bonds and participate in acid-base reactions. Its structure suggests potential applications in medicinal chemistry, particularly in the development of pharmaceuticals, due to the piperidine moiety, which is often found in various bioactive compounds. The compound's molecular weight, solubility, and stability would depend on the specific functional groups and their interactions. Additionally, the presence of chlorine atoms may influence its reactivity and environmental behavior. As with many synthetic organic compounds, safety and handling precautions are essential, given the potential toxicity associated with chlorinated aromatic compounds.

CAS 1042766-55-1

1-[(2,4-DICHLOROPHENYL)METHYL]-2-PIPERIDINECARBOXYLIC ACID

1-[(2,4-Dichlorophenyl)methyl]-2-piperidinecarboxylic acid

Ref: IN-DA01JLDJ