CAS 215878-20-9
:3-(piperidin-4-yl)-1,3-benzoxazol-2(3H)-one
Description:
3-(Piperidin-4-yl)-1,3-benzoxazol-2(3H)-one, with the CAS number 215878-20-9, is a chemical compound characterized by its unique structure, which includes a benzoxazole ring fused with a piperidine moiety. This compound typically exhibits properties associated with both heterocyclic and aromatic compounds, contributing to its potential biological activity. The presence of the piperidine ring suggests that it may interact with various biological targets, potentially influencing neurotransmitter systems or exhibiting pharmacological effects. The benzoxazole component is known for its applications in medicinal chemistry, often associated with anti-inflammatory, antimicrobial, or anticancer activities. The compound's solubility, stability, and reactivity can vary based on its molecular structure and substituents, making it a subject of interest in drug development and synthetic chemistry. Additionally, its specific interactions and effects would require further investigation through experimental studies to elucidate its full potential and applications in various fields, including pharmaceuticals and materials science.
Formula:C12H14N2O2
InChI:InChI=1/C12H14N2O2/c15-12-14(9-5-7-13-8-6-9)10-3-1-2-4-11(10)16-12/h1-4,9,13H,5-8H2
SMILES:c1ccc2c(c1)n(C1CCNCC1)c(=O)o2
Synonyms:- 2(3H)-benzoxazolone, 3-(4-piperidinyl)-
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Found 2 products.
3-(4-Piperidinyl)-1,3-benzoxazol-2(3H)-one
CAS:Formula:C12H14N2O2Purity:97%Color and Shape:SolidMolecular weight:218.25183-(4-Piperidinyl)-1,3-benzoxazol-2(3H)-one
CAS:Formula:C12H14N2O2Purity:95.0%Color and Shape:SolidMolecular weight:218.256

