Identification | More | [Name]
(S)-(-)-alpha-Hydroxy-gamma-butyrolactone | [CAS]
52079-23-9 | [Synonyms]
2,4-DIHYDROXYBUTYRIC ACID LACTONE (3S)-3-HYDROXYDIHYDROFURAN-2(3H)-ONE (S)-2-HYDROXYBUTYROLACTONE (S)-(-)-ALPHA-HYDROXY-GAMMA-BUTYROLACTONE (S)-(-)-DIHYDRO-3-HYDROXY-2(3H)-FURANONE (S)-2-Hydroxy-gamma-butyrolactone 2,4-Dihydroxybutyric acid lactone(S)-2-Hydroxybutyrolactone (S)-(-)-ALPHA-HYDROXY--BUTYROLACTONE (S)-(-)-~-Hydroxy-gamma-butyrolactone, 94% | [Molecular Formula]
C4H6O3 | [MDL Number]
MFCD00211245 | [Molecular Weight]
102.09 | [MOL File]
52079-23-9.mol |
Chemical Properties | Back Directory | [Appearance]
Colourless Liquid | [alpha ]
-68 º (c=1.15 in chloroform) | [Boiling point ]
133 °C10 mm Hg(lit.) | [density ]
1.309 g/mL at 25 °C(lit.)
| [refractive index ]
n20/D 1.467(lit.)
| [Fp ]
>230 °F
| [storage temp. ]
2-8°C | [pka]
13.07±0.20(Predicted) | [Specific Gravity]
1.3 | [optical activity]
[α]23/D 68°, c = 1.15 in chloroform | [CAS DataBase Reference]
52079-23-9(CAS DataBase Reference) |
Hazard Information | Back Directory | [Chemical Properties]
Colourless Liquid | [Uses]
(3S)-3-Hydroxydihydrofuran-2(3H)-one (cas# 52079-23-9) is a compound useful in organic synthesis. | [Uses]
Used to prepare the polyether antibiotic monensin, functionalized D-ring side chains of vitamin D analogs, and pesticides. |
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