| Weight | 115.132 g/mol |
|---|---|
| Formula | C5H9NO2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 1 |
(4R)-4-ethyl-1,3-oxazolidin-2-one (98974-04-0)
4-ethyl-1,3-oxazolidin-2-one · 16112-60-0
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Most-cited Publications
- Enzymatic ammonolysis of ethyl ()-4-chloro-3-hydroxybutanoate. Chemoenzymatic syntheses of both enantiomers of pyrrolidin-3-ol and 5-(chloromethyl)-1,3-oxazolidin-2-one (Tetrahedron-asymmetry, 1999)
- Enzymatic desymmetrization of 2-amino-2-methyl-1,3-propanediol: asymmetric synthesis of (S)-N-Boc-N,O-isopropylidene--methylserinal and (4R)-methyl-4-[2-(thiophen-2-yl)ethyl]oxazolidin-2-one (Tetrahedron-asymmetry, 2005)
- Process for preparing [R-(R*,R*)]-5-(3-chlorophenyl)-3-[2-(3,4-dimethoxylphenyl)-1-methyl-ethyl]-oxazolidin-2-one (1996)
- CHO Hydrogen bonding induced conformation of (S,S)-1,3-benzenedisulfonyl bis[(4S)-4-(ethyl ester)-oxazolidin-2-one] (CrystEngComm, 2005)
Alternate Names
- 4-ethyl-1,3-oxazolidin-2-one
- 16112-60-0
-
SMILESCCC1COC(=O)N1
-
InChIKeyCRHQYASHOICRND-UHFFFAOYSA-N
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