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ChemicalBook--->CAS DataBase List--->51248-35-2

51248-35-2

51248-35-2 Structure

51248-35-2 Structure
IdentificationBack Directory
[Name]

4-isobutyloxazolidine-2,5-dione
[CAS]

51248-35-2
[Synonyms]

ILE-NCA
H-DL-Leu-NCA
Einecs 257-083-3
Isobutyloxazolidine-2,5-dione
4-isobutyloxazolidine-2,5-dione
4-(2-Methylpropyl)-2,5-oxazolidinedione
4-(2-methylpropyl)oxazolidine-2,5-dione
2,5-Oxazolidinedione, 4-(2-methylpropyl)-
Isobutyloxazolidine-2,5-dione[H-DL-Leu-NCA
NCA of N-carboxyanhydride of raceMic DL-leucine
[EINECS(EC#)]

257-083-3
[Molecular Formula]

C7H11NO3
[MDL Number]

MFCD02684167
[MOL File]

51248-35-2.mol
[Molecular Weight]

157.17
Chemical PropertiesBack Directory
[Melting point ]

47-48 °C(Solv: ethyl ether (60-29-7); ligroine (8032-32-4))
[density ]

1.124±0.06 g/cm3(Predicted)
[storage temp. ]

2-8°C
[pka]

9.38±0.40(Predicted)
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
[HS Code ]

2934999090
Hazard InformationBack Directory
[Preparation]

A solution of phosgene(12.5% in toluene, 25 mL, 31.6 mmol) was added to a suspension of l-leucine (1.31 g, 10 mmol) in dioxane (30 mL) and ethyl acetate (25 mL) at 40 ℃ under a static atmosphere of nitrogen. After 4 h, the leucine had dissolved and then the excess phosgene was removed in a stream of nitrogen. The solvent was removed at 40 ℃ in vacuo and the residue was recrystallized from diethyl ether/light petroleum (bp 40–60 ℃) to yield colorless needles of 4-(2-methylpropyl)oxazolidine-2,5-dione (1.01 g, 69%).
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