1-(2-Thienylmethyl)piperidine-4-carbaldehyde is a chemical compound characterized by its unique structure, which includes a piperidine ring substituted with a thienylmethyl group and an aldehyde functional group. The presence of the thienyl moiety, a five-membered aromatic ring containing sulfur, contributes to its potential reactivity and biological activity. The aldehyde group is known for its ability to participate in various chemical reactions, such as condensation and oxidation, making this compound of interest in synthetic organic chemistry. Additionally, the piperidine ring provides a basic nitrogen atom, which can engage in hydrogen bonding and influence the compound's solubility and interaction with biological targets. This compound may exhibit interesting pharmacological properties, making it a candidate for further research in medicinal chemistry. Its specific applications and effects would depend on the context of its use and the biological systems being studied. Overall, 1-(2-thienylmethyl)piperidine-4-carbaldehyde represents a versatile scaffold for the development of novel chemical entities.

1-(2-thienylmethyl)piperidine-4-carbaldehyde

926921-80-4: 1-(2-Thienylmethyl)piperidine-4-carbaldehyde is a chemical compound characterized by its unique structure, which includes a piperidine ring substituted with a thienylmethyl group and an aldehyde functional group. The presence of the thienyl moiety, a five-membered aromatic ring containing sulfur, contributes to its potential reactivity and biological activity. The aldehyde group is known for its ability to participate in various chemical reactions, such as condensation and oxidation, making this compound of interest in synthetic organic chemistry. Additionally, the piperidine ring provides a basic nitrogen atom, which can engage in hydrogen bonding and influence the compound's solubility and interaction with biological targets. This compound may exhibit interesting pharmacological properties, making it a candidate for further research in medicinal chemistry. Its specific applications and effects would depend on the context of its use and the biological systems being studied. Overall, 1-(2-thienylmethyl)piperidine-4-carbaldehyde represents a versatile scaffold for the development of novel chemical entities.

CAS 926921-80-4

1-(2-thienylmethyl)piperidine-4-carbaldehyde

1-[(Thien-2-yl)methyl]piperidine-4-carboxaldehyde

Ref: 54-OR14936

1-(Thiophen-2-ylmethyl)piperidine-4-carbaldehyde

Ref: 10-F777924