| Weight | 163.176 g/mol |
|---|---|
| Formula | C9H9NO2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 1 |
3-Phenyl-2-oxazolidinone (703-56-0)
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- The enzyme-activated irreversible inhibition of type-B monoamine oxidase by 3-(4-[(3-chlorophenyl)methoxy]phenyl)-5-[(methylamino) methyl]-2-oxazolidinone methanesulphonate (compound MD 780236) and the enzyme-catalysed oxidation of this compound as competing reactions. (Biochemical Journal, 1983)
- Enantioselective conjugate additions of aldoximes to 3-crotonoyl-2-oxazolidinone and 1-crotonoyl-3-phenyl-2-imidazolidinone catalyzed by the aqua complex between R,R-DBFOX/Ph and zinc(II) perchlorate (Tetrahedron Letters, 2002)
- Discovery of a Teraryl Oxazolidinone Compound (S)-N-((3-(3-Fluoro-4-(4-(pyridin-2-yl)-1H-pyrazol-1-yl)phenyl)-2-oxooxazolidin-5-yl)methyl)acetamide Phosphate as a Novel Antimicrobial Agent with Enhanced Safety Profile and Efficacies (Journal of Medicinal Chemistry, 2015)
- Research on compounds with antiblastic activity. XL. Synthesis of 3-p-(2',5'-dimethoxy-4'-(N,N-bis-( -chloroethyl)-amino)benzylideneamino)phenyl-2-oxazolidinone (GEA 29 ; BAY a 5850) and its analogues. (Il Farmaco; edizione scientifica, 1971)
- Diastereoselective Aldol Condensation Using a Chiral Oxazolidinone Auxiliary: (2S*,3S*)3Hydroxy3phenyl2methylpropanoic Acid (Organic Syntheses, 2003)
- Thermodynamic properties of 3-phenyl-5-phenoxymethyl-2-oxazolidinone and 3-phenyl-5-phenoxymethyl-2-N-phenyliminooxazolidine between O and 330 K (Russian Chemical Bulletin, 1987)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1COC(=O)N1C2=CC=CC=C2
-
InChIKeyNCTCGHLIHJJIBK-UHFFFAOYSA-N
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N-(2-Chloroethyl)aniline
(Ester from carboxilic acid(SN2))
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