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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
InChI
1S/C10H23O5P/c1-5-12-10(13-6-2)9-16(11,14-7-3)15-8-4/h10H,5-9H2,1-4H3
InChIKey
LUQYELQXRPNKRY-UHFFFAOYSA-N
SMILES
CCOC(CP(=O)(OCC)OCC)OCC
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
RIDADR 
UN2810
WGK Germany 
3
21
HazardClass 
6.1
HS Code 
29319090
Storage Class
10 - Combustible liquids
Hazard Classifications
Eye Irrit. 2
Skin Irrit. 2
STOT SE 3

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.

reaction suitability

reaction type: C-C Bond Formation

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