| Weight | 204.273 g/mol |
|---|---|
| Formula | C12H16N2O |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 2 |
N-Piperidin-4-yl-benzamide (33953-37-6)
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- Radiolabeling of a high potency cannabinoid subtype-1 receptor ligand, N-(4-fluoro-benzyl)-4-(3-(piperidin-1-yl)-indole-1-sulfonyl)benzamide (PipISB), with carbon-11 or fluorine-18 (Journal of Labelled Compounds and Radiopharmaceuticals, 2008)
- Synthesis and structureactivity relationships of N-{1-[(6-fluoro-2-naphthyl)methyl]piperidin-4-yl}benzamide derivatives as novel CCR3 antagonists (Bioorganic & Medicinal Chemistry, 2008)
- N,N-Diethyl-4-[(3-hydroxyphenyl)(piperidin-4-yl)amino] benzamide derivatives: The development of diaryl amino piperidines as potent opioid receptor agonists with in vivo anti-nociceptive activity in rodent models (Bioorganic & Medicinal Chemistry Letters, 2009)
- Crystal structure of 4-methyl-N-[2-(piperidin-1-yl)eth-yl]benzamide monohydrate. (Acta Crystallographica Section E: Crystallographic Communications, 2015)
- Corrigendum to Synthesis and structureactivity relationships of N-{1-[(6-fluoro-2-naphthyl)methyl]piperidin-4-yl}benzamide derivatives as novel CCR3 antagonists [Bioorg. Med. Chem. 16 (2008) 144156] (Bioorganic & Medicinal Chemistry, 2008)
- N-[(1-Benzoylpiperidin-4-yl)methyl]benzamide (Acta Crystallographica Section E-structure Reports Online, 2014)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1CNCCC1NC(=O)C2=CC=CC=C2
-
InChIKeyJMQDNLCNCDSHNC-UHFFFAOYSA-N
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Synthesis
Reactant
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n-(3-aminopropyl)benzamide
(Reductive amination)
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N-Piperidin-4-yl-benzamide
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