ChemicalBook--->CAS DataBase List--->26654-39-7

26654-39-7

26654-39-7 Structure

26654-39-7 Structure
IdentificationBack Directory
[Name]

4,4-DIMETHYL-2-OXAZOLIDINONE
[CAS]

26654-39-7
[Synonyms]

DMO
DMRTA1
4,4-Dimethyloxazolidinone
4,4-dimethyl-oxazolidin-2...
4,4-DIMETHYL-2-OXAZOLIDINONE
2-Oxazolidinone,4,4-dimethyl-
4,4-diMethyl-oxazolidin-2-one
4,4-dimethyl-oxazolidine-2-one
4,4-Dimethyl-1,3-oxazolidin-2-one
4,4-DIMETHYL-2-OXAZOLIDINONE STANDARD
ANTI-DMRTA1 (C-TERM) antibody produced in rabbit
Doublesex- and mab-3-related transcription factor A1
[Molecular Formula]

C5H9NO2
[MDL Number]

MFCD04038702
[MOL File]

26654-39-7.mol
[Molecular Weight]

115.13
Chemical PropertiesBack Directory
[Melting point ]

55-56 °C(Solv: ethanol (64-17-5); ligroine (8032-32-4))
[Boiling point ]

152-154 °C(Press: 10 Torr)
[density ]

1.039±0.06 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,Room Temperature
[form ]

solid
[pka]

12.91±0.40(Predicted)
[color ]

White to off-white
[InChI]

1S/C5H9NO2/c1-5(2)3-8-4(7)6-5/h3H2,1-2H3,(H,6,7)
[InChIKey]

SYARCRAQWWGZKY-UHFFFAOYSA-N
[SMILES]

CC1(C)COC(=O)N1
[EPA Substance Registry System]

2-Oxazolidinone, 4,4-dimethyl- (26654-39-7)
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H317
[Precautionary statements ]

P280
[WGK Germany ]

3
[TSCA ]

TSCA listed
[HS Code ]

2934999090
[Storage Class]

11 - Combustible Solids
Spectrum DetailBack Directory
[Spectrum Detail]

4,4-DIMETHYL-2-OXAZOLIDINONE(26654-39-7)1HNMR
Hazard InformationBack Directory
[Synthesis]

2-Amino-2-methyl-1-propanol

124-68-5

Urea

57-13-6

4,4-DIMETHYL-2-OXAZOLIDINONE

26654-39-7

4,4-Dimethyloxazolidin-2-one (DMO) was synthesized as follows: 2-amino-2-methyl-1-propanol (10.0 g, 112 mmol) was mixed with urea (13.5 g, 224 mmol), and the mixture was heated and reacted for 1 hour at 170-180 °C, followed by heating up to 210-220 °C and continued heating for 1 hour. After completion of the reaction, it was cooled to room temperature and the reaction mixture was dissolved in water (50 mL). Dichloromethane (DCM, 5 x 50 mL) extraction was performed with the aqueous solution. The organic phases were combined, dried with anhydrous sodium sulfate (Na2SO4), filtered and concentrated under reduced pressure to afford 4,4-dimethyloxazolidin-2-one 10.3 g in 80% yield. The product was identified by 1H NMR (CDCl3): δ 6.13 (br s, 1H, NH), 4.07 (s, 2H, CH2), 1.32 (s, 6H, 2 CH3) ppm; 13C NMR (CDCl3) δ 159.4,77.1,55.4,27.7 ppm.

[References]

[1] Asian Journal of Chemistry, 2011, vol. 23, # 2, p. 929 - 930
[2] Patent: WO2015/68159, 2015, A2. Location in patent: Paragraph 00121-00122
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