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DIETHYL 2,2-DIETHOXYETHYLPHOSPHONATE

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DIETHYL 2,2-DIETHOXYETHYLPHOSPHONATE Basic information

Product Name:
DIETHYL 2,2-DIETHOXYETHYLPHOSPHONATE
Synonyms:
  • Phosphonic acid, (2,2-diethoxyethyl)-, diethyl ester
  • DIETHYL PHOSPHONOACETALDEHYDE DIETHYL ACETAL
  • DIETHYL PHOSPHONACETALDEHYDE DIETHYL ACETAL
  • DIETHYL 2,2-DIETHOXETHYLPHOSPHONATE
  • DIETHYL 2,2-DIETHOXY-ETHANEPHOSPHONATE
  • DIETHYL 2,2-DIETHOXYETHYLPHOSPHONATE
  • AURORA KA-1450
  • Diethyl phosphonoacetaldehyde diethyl acetal, 90%, tech.
CAS:
7598-61-0
MF:
C10H23O5P
MW:
254.26
EINECS:
231-504-0
Product Categories:
  • Wittig Reagents
  • Horner-Emmons Reaction
  • Synthetic Organic Chemistry
  • Wittig & Horner-Emmons Reaction
Mol File:
7598-61-0.mol
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DIETHYL 2,2-DIETHOXYETHYLPHOSPHONATE Chemical Properties

Boiling point:
146-149 °C14 mm Hg(lit.)
Density 
1.052 g/mL at 25 °C(lit.)
refractive index 
n20/D 1.430(lit.)
Flash point:
>230 °F
storage temp. 
2-8°C
solubility 
Chloroform, Dichloromethane
form 
Oil
color 
Colourless
Water Solubility 
Soluble in chloroform and dichloromethane. Not miscible or difficult to mix in water.
Sensitive 
Moisture Sensitive
BRN 
1785614
CAS DataBase Reference
7598-61-0(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-37/39
WGK Germany 
3
21
HS Code 
29319090

MSDS

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DIETHYL 2,2-DIETHOXYETHYLPHOSPHONATE Usage And Synthesis

Chemical Properties

Colourless Oil

Uses

Diethyl 2,2-diethoxyethylphosphonate is used reactant for synthesis of α,β-alkenal derivatives by two-carbon homologation, lower rim-phosphonylated rexorcinol calix[4]arenes by condensation reactions, α-Phosphovinyl radicals via a radical trapping sequence, inhibitors of reverse transcriptase via 1,3-dipolar cycloadditions and for Friedel-Crafts reactions.

Uses

Reactant for synthesis of:

  • α,β-Alkenal derivatives by two-carbon homologation
  • Lower rim-phosphonylated rexorcinol calix[4]arenes by condensation reactions
  • α-Phosphovinyl radicals via a radical trapping sequence
  • Inhibitors of reverse transcriptase via 1,3-dipolar cycloadditions

Reactant for Friedel-Crafts reactions

Uses

Diethyl 2,2-diethoxyethylphosphonate can be used as a useful wittig reagent.

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