4,4-DIMETHYL-2-OXAZOLIDINONE

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Products Intro: Product Name:4,4-Dimethyl-1,3-oxazolidin-2-one
CAS:26654-39-7
Purity:NLT 98% Package:1G;1KG;100KG
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Products Intro: Product Name:4,4-dimethyl-oxazolidin-2-one
CAS:26654-39-7
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Products Intro: Product Name:4,4-DIMETHYL-2-OXAZOLIDINONE
CAS:26654-39-7
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CAS:26654-39-7
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Products Intro: Product Name:4,4-DIMETHYL-2-OXAZOLIDINONE
CAS:26654-39-7
Purity:0.99 Package:10MG,50MG,100MG,1G

4,4-DIMETHYL-2-OXAZOLIDINONE manufacturers

4,4-DIMETHYL-2-OXAZOLIDINONE Basic information
Product Name:4,4-DIMETHYL-2-OXAZOLIDINONE
Synonyms:4,4-dimethyl-oxazolidin-2...;4,4-diMethyl-oxazolidin-2-one;ANTI-DMRTA1 (C-TERM) antibody produced in rabbit;DMRTA1;Doublesex- and mab-3-related transcription factor A1;DMO;4,4-DIMETHYL-2-OXAZOLIDINONE;4,4-Dimethyl-1,3-oxazolidin-2-one
CAS:26654-39-7
MF:C5H9NO2
MW:115.13
EINECS:
Product Categories:
Mol File:26654-39-7.mol
4,4-DIMETHYL-2-OXAZOLIDINONE Structure
4,4-DIMETHYL-2-OXAZOLIDINONE Chemical Properties
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
pka12.91±0.40(Predicted)
form solid
color White to off-white
InChI1S/C5H9NO2/c1-5(2)3-8-4(7)6-5/h3H2,1-2H3,(H,6,7)
InChIKeySYARCRAQWWGZKY-UHFFFAOYSA-N
SMILESCC1(C)COC(=O)N1
EPA Substance Registry System2-Oxazolidinone, 4,4-dimethyl- (26654-39-7)
Safety Information
WGK Germany 3
TSCA TSCA listed
HS Code 2934999090
Storage Class11 - Combustible Solids
MSDS Information
4,4-DIMETHYL-2-OXAZOLIDINONE Usage And Synthesis
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
4,4-DIMETHYL-2-OXAZOLIDINONE Preparation Products And Raw materials
Raw materialsisobutyl carbamate-->1,1'-Thiocarbonyldiimidazole-->Ethyl chloroformate-->carbon monoxide-->2-Amino-2-methyl-1-propanol-->Urea-->Dimethyl carbonate-->Diethyl carbonate-->Diphosgene
Tag:4,4-DIMETHYL-2-OXAZOLIDINONE(26654-39-7) Related Product Information
(-)-CHIRACAMPHOX 4,4-DIMETHYL-2-OXAZOLIDINONE 3-BROMO-4,4-DIMETHYL-2-OXAZOLIDINONE 1,1-CYCLOHEXANO-8-METHOXY-11B-METHYL-5,6,11,11B-TETRAHYDRO-1H-[1,3]OXAZOLO[3',4':1,2]PYRIDO[3,4-B]INDOL-3-ONE 1-ETHYL-1,10B-DIMETHYL-1,5,6,10B-TETRAHYDRO[1,3]OXAZOLO[4,3-A]ISOQUINOLIN-3-ONE SPECS AG-205/37268014 CBI-BB ZERO/005436 2A,5,5,10B-TETRAMETHYL-3,4,4A,5,10,10B-HEXAHYDRO-2AH-2-OXA-10A-AZABENZO[G]CYCLOPENTA[CD]AZULEN-1-ONE CBI-BB ZERO/005643 4,4,6A,6B-TETRAMETHYLHEXAHYDRO-3H-1-OXA-2A,3-DIAZACYCLOPENTA[CD]PENTALEN-2-ONE 8,9-DIMETHOXY-1,1,10B-TRIMETHYL-1,5,6,10B-TETRAHYDRO[1,3]OXAZOLO[4,3-A]ISOQUINOLIN-3-ONE 3A,9B-DIMETHYL-3A,4,5,9B-TETRAHYDRONAPHTHO[1,2-D][1,3]OXAZOL-2(1H)-ONE CBI-BB ZERO/001967 CBI-BB ZERO/003104 1,1,10,10,10A-PENTAMETHYL-5,6,10,10A-TETRAHYDRO-1H-DI[1,3]OXAZOLO[3,4-D:4,3-G][1,4]DIAZEPINE-3,8-DIONE 4,4,6A,6B-TETRAMETHYL-3-PHENYLHEXAHYDRO-3H-1-OXA-2A,3-DIAZACYCLOPENTA[CD]PENTALEN-2-ONE 1-ETHYL-8,9-DIMETHOXY-1,10B-DIMETHYL-1,5,6,10B-TETRAHYDRO[1,3]OXAZOLO[4,3-A]ISOQUINOLIN-3-ONE

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