CAS 893745-85-2
:4-(piperidin-1-ylmethyl)thiophene-2-carbaldehyde
Description:
4-(Piperidin-1-ylmethyl)thiophene-2-carbaldehyde is an organic compound characterized by its thiophene ring, which is a five-membered aromatic heterocycle containing sulfur. The presence of a piperidine group, a six-membered nitrogen-containing ring, contributes to its potential biological activity and solubility properties. This compound features an aldehyde functional group, which is known for its reactivity, particularly in condensation reactions and as a precursor in various synthetic pathways. The molecular structure suggests that it may exhibit properties such as moderate polarity due to the combination of the hydrophobic thiophene and the more polar piperidine and aldehyde functionalities. Its applications may extend to medicinal chemistry, where it could serve as a building block for the synthesis of more complex molecules or as a potential pharmacophore in drug development. Additionally, the compound's unique structure may impart specific interactions with biological targets, making it of interest in the fields of organic synthesis and medicinal chemistry.
Formula:C11H15NOS
InChI:InChI=1/C11H15NOS/c13-8-11-6-10(9-14-11)7-12-4-2-1-3-5-12/h6,8-9H,1-5,7H2
SMILES:C1CCN(CC1)Cc1cc(C=O)sc1
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Found 3 products.
4-(Piperidin-1-ylmethyl)thiophene-2-carbaldehyde
CAS:<p>4-(Piperidin-1-ylmethyl)thiophene-2-carbaldehyde</p>Purity:≥95%Molecular weight:209.31g/mol4-(Piperidin-1-ylmethyl)thiophene-2-carbaldehyde
CAS:<p>Versatile small molecule scaffold</p>Formula:C11H15NOSPurity:Min. 95%Molecular weight:209.3 g/mol


