| Weight | 165.192 g/mol |
|---|---|
| Formula | C9H11NO2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 3 |
2-(4-Methoxyphenyl)acetamide (6343-93-7)
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- Sigma-Aldrich - 2-(4-Methoxyphenyl)acetamide30.00 USD
- Fisher Scientific - Search for 2-(4-Methoxyphenyl)acetamide
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- Discovery of (S)-N-{2-[1-(3-Ethoxy-4-methoxyphenyl)-2-methanesulfonylethyl]-1,3-dioxo-2,3-dihydro-1H-isoindol-4-yl}acetamide (Apremilast), a Potent and Orally Active Phosphodiesterase 4 and Tumor Necrosis Factor- Inhibitor (Journal of Medicinal Chemistry, 2009)
- MF498 [N-{[4-(5,9-Diethoxy-6-oxo-6,8-dihydro-7H-pyrrolo[3,4-g]quinolin-7-yl)-3-methylbenzyl]sulfonyl}-2-(2-methoxyphenyl)acetamide], a Selective E Prostanoid Receptor 4 Antagonist, Relieves Joint Inflammation and Pain in Rodent Models of Rheumatoid and Osteoarthritis (Journal of Pharmacology and Experimental Therapeutics, 2008)
- Pharmacological Characterization of AC-90179 [2-(4-Methoxyphenyl)-N-(4-methyl-benzyl)-N-(1-methyl-piperidin-4-yl)-acetamide Hydrochloride]: A Selective Serotonin 2A Receptor Inverse Agonist (Journal of Pharmacology and Experimental Therapeutics, 2004)
- Discovery of 2-(6-(5-Chloro-2-methoxyphenyl)-4-oxo-2-thioxo-3,4-dihydropyrimidin-1(2H)-yl)acetamide (PF-06282999): A Highly Selective Mechanism-Based Myeloperoxidase Inhibitor for the Treatment of Cardiovascular Diseases. (Journal of Medicinal Chemistry, 2015)
- Crystalline forms of 2,2,2-trifluoro-N-[(1R,2S)-1-{[1-(4-fluorophenyl)-1H-indazol-5-yl]oxy}-1-(3-methoxyphenyl)-2-propanyl]acetamide (AZD-5423) (Expert Opinion on Therapeutic Patents, 2013)
- Bischler-Napieralski Cyclization of N-[2-(2-Bromo-5-hydroxy-4-methoxyphenyl)-ethyl]-N-[(S)-1-phenylethyl]2-(2-bromo-4,5-dimethoxyphenyl)acetamide Accompanied by Elimination of Chiral Auxiliary (Heterocycles, 2001)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCOC1=CC=C(C=C1)CC(=O)N
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InChIKeyOLKQIWCQICCYQS-UHFFFAOYSA-N
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