Benzyl 3-(chlorocarbonyl)tetrahydro-1(2H)-pyridinecarboxylate is a chemical compound characterized by its complex structure, which includes a tetrahydropyridine ring and a benzyl group. The presence of the chlorocarbonyl functional group indicates that it can participate in nucleophilic acyl substitution reactions, making it a potentially reactive compound in organic synthesis. This compound is likely to exhibit moderate to high polarity due to the presence of both ester and carbonyl functionalities, which can influence its solubility in various solvents. Additionally, the tetrahydropyridine moiety may impart basic properties, allowing it to engage in various chemical reactions, including those involving electrophiles. The compound's molecular structure suggests potential applications in medicinal chemistry, particularly in the development of pharmaceuticals, due to the presence of the pyridine ring, which is often found in biologically active molecules. Safety and handling precautions should be observed, as compounds containing chlorine and carbonyl groups can pose health risks and environmental concerns.

benzyl 3-(chlorocarbonyl)tetrahydro-1(2H)-pyridinecarboxylate

216502-94-2: Benzyl 3-(chlorocarbonyl)tetrahydro-1(2H)-pyridinecarboxylate is a chemical compound characterized by its complex structure, which includes a tetrahydropyridine ring and a benzyl group. The presence of the chlorocarbonyl functional group indicates that it can participate in nucleophilic acyl substitution reactions, making it a potentially reactive compound in organic synthesis. This compound is likely to exhibit moderate to high polarity due to the presence of both ester and carbonyl functionalities, which can influence its solubility in various solvents. Additionally, the tetrahydropyridine moiety may impart basic properties, allowing it to engage in various chemical reactions, including those involving electrophiles. The compound's molecular structure suggests potential applications in medicinal chemistry, particularly in the development of pharmaceuticals, due to the presence of the pyridine ring, which is often found in biologically active molecules. Safety and handling precautions should be observed, as compounds containing chlorine and carbonyl groups can pose health risks and environmental concerns.

CAS 216502-94-2

benzyl 3-(chlorocarbonyl)tetrahydro-1(2H)-pyridinecarboxylate

1-Benzyloxycarbonylpiperidine-3-carbonyl chloride

Ref: IN-DA007PNP

3-(Chlorocarbonyl)piperidine, N-CBZ protected

Ref: 54-OR23395

1-Benzyloxycarbonylpiperidine-3-carbonyl chloride

Ref: 10-F017175