| Weight | 147.177 g/mol |
|---|---|
| Formula | C9H9NO |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 2 |
N-Phenylacrylamide (2210-24-4)
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- (S)-N-[1-(3-morpholin-4-ylphenyl)ethyl]- 3-phenylacrylamide: an orally bioavailable KCNQ2 opener with significant activity in a cortical spreading depression model of migraine. (Journal of Medicinal Chemistry, 2003)
- Water soluble copolymers: 38. Synthesis and characterization of electrolyte responsive terpolymers of acrylamide, N-(4-butyl)phenylacrylamide, and sodium acrylate, sodium-2-acrylamido-2-methylpropanesulphonate or sodium-3-acrylamido-3-methylbutanoate (Polymer, 1992)
- Synthesis and rheological behavior of poly[acrylamideacrylic acidN-(4-butyl)phenylacrylamide] hydrophobically modified polyelectrolytes (Colloid and Polymer Science, 2004)
- N-phenylacrylamide functional polymer with high affinity for ochratoxin A (Reactive & Functional Polymers, 2004)
- Highly Phosphonated Poly(N-phenylacrylamide) for Proton Exchange Membranes (Journal of Polymer Science Part A, 2011)
- Synthesis, biological evaluation and molecular docking studies of 3-(1,3-diphenyl-1H-pyrazol-4-yl)-N-phenylacrylamide derivatives as inhibitors of HDAC activity (Bioorganic & Medicinal Chemistry, 2012)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC=CC(=O)NC1=CC=CC=C1
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InChIKeyBPCNEKWROYSOLT-UHFFFAOYSA-N
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Synthesis
Reactant
+
1-Hydroxy-1,2-benziodoxol-3(1H)-one 1-oxide
(Nicolaou IBX dehydrogenation)
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N-Phenylacrylamide
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