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1,1-Dioxo-tetrahydro-thiopyran-4-one

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1,1-Dioxo-tetrahydro-thiopyran-4-one Basic information

Product Name:
1,1-Dioxo-tetrahydro-thiopyran-4-one
Synonyms:
  • 1,1-Dioxo-tetrahydro-thiopyran-4-one
  • 1,1-DIOXO-TETRAHYDRO-1LAMBDA*6*-THIOPYRAN-4-ONE
  • 4-Oxotetrahydro-2H-thiopyran 1,1-dioxide
  • Tetrahydro-4-oxo-4H-thiopyran 1,1-dioxide
  • 4-Tetrahydrothiopyranone 1,1-dioxide
  • 1,1-Dioxo-tetrahydro-2H-thiopyran-4-one
  • tetrahydro-1λ6-thiopyran-1,1,4-trione
  • 1,1-dioxo-4-thianone
CAS:
17396-35-9
MF:
C5H8O3S
MW:
148.18
EINECS:
214-015-7
Mol File:
17396-35-9.mol
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1,1-Dioxo-tetrahydro-thiopyran-4-one Chemical Properties

Melting point:
170.0 to 174.0 °C
Boiling point:
385.2±35.0 °C(Predicted)
Density 
1.352±0.06 g/cm3(Predicted)
storage temp. 
Inert atmosphere,Room Temperature
form 
powder to crystal
color 
White to Almost white
λmax
290nm(EtOH)(lit.)
InChI
InChI=1S/C5H8O3S/c6-5-1-3-9(7,8)4-2-5/h1-4H2
InChIKey
XFMQGQAAHOGFQS-UHFFFAOYSA-N
SMILES
C1S(=O)(=O)CCC(=O)C1
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Safety Information

Risk Statements 
43
Safety Statements 
36/37
HazardClass 
IRRITANT
HS Code 
2932990090
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1,1-Dioxo-tetrahydro-thiopyran-4-one Usage And Synthesis

Synthesis

1072-72-6

17396-35-9

The general procedure for the synthesis of tetrahydrothiopyran-4-one 1,1-dioxide from tetrahydrothiopyran-4-one was as follows: in Example 22, to a stirred solution of tetrahydrothiopyran-4-one (5.30 g, 43.1 mmol, Aldrich) in 50 mL of ethyl acetate, 32% peracetic acid (24 g, 110 mmol) was added dropwise at a slow rate, taking care to avoid refluxing. After completion of the dropwise addition, the reaction mixture was cooled to room temperature and the solid was collected by filtration to afford 1,1-dioxo-tetrahydro-thiopyran-4-one as a white solid (5.69 g, 89% yield).

References

[1] Journal of Organic Chemistry, 1995, vol. 60, # 6, p. 1665 - 1673
[2] Patent: US2007/129416, 2007, A1. Location in patent: Page/Page column 19/1
[3] Patent: EP2261213, 2010, A1. Location in patent: Page/Page column 60
[4] Journal of Organic Chemistry, 1998, vol. 63, # 24, p. 8952 - 8956
[5] European Journal of Medicinal Chemistry, 1999, vol. 34, # 2, p. 125 - 135

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