| Weight | 151.165 g/mol |
|---|---|
| Formula | C8H9NO2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 3 |
2-Phenoxyacetamide (621-88-5)
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- A Novel Allosteric Potentiator of AMPA Receptors: 4-[2-(Phenylsulfonylamino)ethylthio]-2,6-Difluoro-Phenoxyacetamide (The Journal of Neuroscience, 1997)
- Design, synthesis and structure-activity relationship studies of novel phenoxyacetamide-based free fatty acid receptor 1 agonists for the treatment of type 2 diabetes. (Bioorganic & Medicinal Chemistry, 2015)
- Potentiating effects of 4-[2-(phenylsulfonylamino)ethylthio]-2,6-difluoro-phenoxyacetamide (PEPA) on excitatory synaptic transmission in dentate granule cells (Neuroscience Research, 1999)
- Substituted N-sulfonylaminobenzyl-2-phenoxyacetamide compounds as VR1 receptor agonists (2005)
- Synthesis and Herbicidal Activity of Novel N-(2-Fluoro-5(3-methyl-2,6-dioxo-4-(trifluoromethyl)-2,3-dihydro-pyrimidin-1(6H)-yl)phenyl)-2-phenoxyacetamide Derivatives (Chinese Journal of Chemistry, 2011)
- Micellar catalysis of the basic hydrolysis of N-methyl-N-(4'-nitropheny1)-2-phenoxyacetamide. Variation of the magnitude of catalysis for differentsources of hydroxide ions (Australian Journal of Chemistry, 1981)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CC=C(C=C1)OCC(=O)N
-
InChIKeyAOPRXJXHLWYPQR-UHFFFAOYSA-N
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