1-Piperidineethanethiol, with the CAS number 4706-22-3, is an organic compound characterized by the presence of a piperidine ring and a thiol functional group. This compound features a six-membered nitrogen-containing heterocycle (piperidine) attached to an ethyl chain that terminates in a thiol (-SH) group. The presence of the thiol group imparts distinctive properties, such as a strong, often unpleasant odor, and the ability to form disulfide bonds, which can influence its reactivity and interactions with other molecules. 1-Piperidineethanethiol is typically a colorless to pale yellow liquid and is soluble in organic solvents. It is used in various applications, including as a building block in organic synthesis and in the development of pharmaceuticals. The compound's reactivity is influenced by the nucleophilic nature of the thiol group, allowing it to participate in various chemical reactions, such as nucleophilic substitutions and the formation of metal thiolate complexes. Safety precautions should be observed when handling this compound due to its potential toxicity and irritant properties.

1-Piperidineethanethiol

4706-22-3: 1-Piperidineethanethiol, with the CAS number 4706-22-3, is an organic compound characterized by the presence of a piperidine ring and a thiol functional group. This compound features a six-membered nitrogen-containing heterocycle (piperidine) attached to an ethyl chain that terminates in a thiol (-SH) group. The presence of the thiol group imparts distinctive properties, such as a strong, often unpleasant odor, and the ability to form disulfide bonds, which can influence its reactivity and interactions with other molecules. 1-Piperidineethanethiol is typically a colorless to pale yellow liquid and is soluble in organic solvents. It is used in various applications, including as a building block in organic synthesis and in the development of pharmaceuticals. The compound's reactivity is influenced by the nucleophilic nature of the thiol group, allowing it to participate in various chemical reactions, such as nucleophilic substitutions and the formation of metal thiolate complexes. Safety precautions should be observed when handling this compound due to its potential toxicity and irritant properties.

CAS 4706-22-3

1-Piperidineethanethiol

2-(Piperidin-1-yl)ethane-1-thiol

Ref: 3D-EAA70622