ChemicalBook--->CAS DataBase List--->1158098-73-7

1158098-73-7

1158098-73-7 Structure

1158098-73-7 Structure
IdentificationBack Directory
[Name]

2-Methyl-N-(oxetan-3-ylid...
[CAS]

1158098-73-7
[Synonyms]

2-Methyl-N-(oxetan-3-ylid...
2-Methyl-N-(oxetan-3-ylidene)
3-[(tert-Butylsulfinyl)imino]oxetan
3-(tert-butylsulfinylmethylene)oxetane
2-Methyl-n-(oxetan-3-yl)propane-2-sulfinaMide
2-Methyl-N-(3-oxetanylidene)-2-propanesulfinaMide
2-PropanesulfinaMide, 2-Methyl-N-3-oxetanylidene-
2-Methyl-N-(oxetan-3-ylidene)propane-2-sulfinamide
2-Methyl-N-(3-oxetanylidene)propane-2-sulfinamide,95%
2-Methyl-N-(3-oxetanylidene)propane-2-sulfinaMide, 95%
2-Methyl-N-(oxetan-3-ylidene)propane-2-sulfinaMide 2-Methylpropane-2-sulfinic acid oxetan-3-ylideneaMide
[Molecular Formula]

C7H13NO2S
[MDL Number]

MFCD14702522
[MOL File]

1158098-73-7.mol
[Molecular Weight]

175.249
Chemical PropertiesBack Directory
[Boiling point ]

302.8±52.0 °C(Predicted)
[density ]

1.25
[storage temp. ]

under inert gas (nitrogen or Argon) at 2-8°C
[pka]

-0.50±0.20(Predicted)
[Appearance]

Light yellow to brown Solid-Liquid Mixture
[Water Solubility ]

Soluble in water. (1.00E+06 mg/L).
[InChI]

InChI=1S/C7H13NO2S/c1-7(2,3)11(9)8-6-4-10-5-6/h4-5H2,1-3H3
[InChIKey]

VKUZMNXQGKBLHN-UHFFFAOYSA-N
[SMILES]

CC(C)(S(/N=C1\COC\1)=O)C
[CAS DataBase Reference]

1158098-73-7
Safety DataBack Directory
[Hazard Codes ]

F,C
[Risk Statements ]

36/37/38
[Safety Statements ]

26-37-60
[TSCA ]

No
[HS Code ]

2932990090
Hazard InformationBack Directory
[Uses]

It is an important raw material and intermediate used in organic synthesis, pharmaceuticals, agrochemicals and dyestuffs.
[Synthesis]

3-Oxetanone

6704-31-0

tert-Butanesulfinamide

146374-27-8

2-Propanesulfinamide, 2-methyl-N-3-oxetanylidene-

1158098-73-7

3-Oxetanone (0.5 g, 7 mmol) and tert-butylsulfinamide (0.9 g, 7 mmol) were dissolved in ethanol (30 mL), titanium tetraisopropoxide (2 g, 7 mmol) was added, and the reaction was stirred for 8 hours at 80 °C. After the reaction was completed, 1N sodium hydroxide solution (10 mL) was added and stirring was continued for 2 hours at room temperature. The reaction mixture was concentrated to dryness and the resulting crude product was purified by silica gel column chromatography to give the final target product 3-[(tert-butylsulfinylidene)imino]oxetane (0.6 g, 76% yield) in white solid form.

[References]

[1] Organic Letters, 2011, vol. 13, # 15, p. 3912 - 3915
[2] Patent: CN108341814, 2018, A. Location in patent: Paragraph 0217-0218; 0220-0222
[3] Patent: US2012/108574, 2012, A1. Location in patent: Page/Page column 115
[4] Patent: EP3342765, 2018, A1. Location in patent: Paragraph 0231
[5] Patent: WO2012/13643, 2012, A1. Location in patent: Page/Page column 64
Spectrum DetailBack Directory
[Spectrum Detail]

2-Methyl-N-(oxetan-3-ylid...(1158098-73-7)1HNMR
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