Basic information Safety Supplier Related

1,4-DIOXA-SPIRO[4.5]DECAN-8-OL

Basic information Safety Supplier Related

1,4-DIOXA-SPIRO[4.5]DECAN-8-OL Basic information

Product Name:
1,4-DIOXA-SPIRO[4.5]DECAN-8-OL
Synonyms:
  • 4-HYDROXYCYCLOHEXANONE MONOETHYLENE KETAL
  • 1,4-DIOXA-SPIRO[4.5]DECAN-8-OL
  • 4,4-Ethylenedioxycyclohexanol.
  • 4-Hydroxycyclohexanone ethylene acetal, 90+%
  • 4,4-(Ethylenebisoxy)cyclohexanol
  • 1,4-Dioxaspiro[4.5]decan-8-ol,98%
  • 4-Dioxaspiro[4.5]decan-8-ol
  • 4-Hydroxycyclohexanone ethylene acetal
CAS:
22428-87-1
MF:
C8H14O3
MW:
158.2
Product Categories:
  • Miscellaneous
Mol File:
22428-87-1.mol
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1,4-DIOXA-SPIRO[4.5]DECAN-8-OL Chemical Properties

Boiling point:
103-104 °C(Press: 0.55 Torr)
Density 
1.17±0.1 g/cm3(Predicted)
refractive index 
1.485-1.487
storage temp. 
Inert atmosphere,2-8°C
pka
15.11±0.20(Predicted)
form 
Viscous Liquid
color 
Clear colorless
InChI
InChI=1S/C8H14O3/c9-7-1-3-8(4-2-7)10-5-6-11-8/h7,9H,1-6H2
InChIKey
HKQTYQDNCKMNHZ-UHFFFAOYSA-N
SMILES
O1C2(CCC(O)CC2)OCC1
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Safety Information

Hazard Codes 
Xi
Safety Statements 
24/25
HazardClass 
IRRITANT
HS Code 
29339900

MSDS

  • Language:English Provider:ACROS
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1,4-DIOXA-SPIRO[4.5]DECAN-8-OL Usage And Synthesis

Chemical Properties

clear colorless viscous liquid

Uses

1,4-Dioxaspiro[4.5]decan-8-ol can be used to synthesize pharmaceutical compounds such as diuretics.

Synthesis

4746-97-8

22428-87-1

Step A: Preparation of 4-dioxaspiro[4.5]decan-8-ol 1,4-Cyclohexanedione monoethylene glycol ketal (5.0134 g, 32.10 mmol) was dissolved in methanol (100 mL) and cooled in an ice bath. Sodium borohydride (3.64 g, 96.30 mmol) was added to the solution in batches over 20 min. The reaction mixture was stirred at 0 °C for 30 min, then slowly warmed to room temperature and continued stirring for 1 h. The reaction mixture was then stirred at 0 °C for 1 h. The reaction mixture was then stirred at 0 °C for 1 h. Upon completion of the reaction, 4-hydroxycyclohexanone ethylene glycol acetal (5.56 g, 109% yield) was obtained by a standard post-processing step, the product was a yellow oil and could be used in subsequent reactions without further purification. The structure of the product was confirmed by 1H NMR (400 MHz, chloroform-D): δ 1.47-1.70 (m, 5H), 1.72-1.92 (m, 4H), 3.70-3.83 (m, 1H), 3.85-3.96 (m, 4H).

References

[1] Journal of Medicinal Chemistry, 1992, vol. 35, # 12, p. 2243 - 2247
[2] Journal of the American Chemical Society,
[3] Journal of the American Chemical Society, 2009, vol. 131, p. 251 - 262
[4] Patent: US2009/275574, 2009, A1. Location in patent: Page/Page column 16
[5] Patent: WO2013/30665, 2013, A1. Location in patent: Page/Page column 175; 176

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