| Weight | 224.193 g/mol |
|---|---|
| Formula | C8H17O5P |
| Hydrogen Acceptors | 5 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 7 |
Triethyl phosphonoacetate (867-13-0, 30492-56-9)
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- Structures and Magnetic Properties of a Series of Metal Phosphonoacetates Synthesized from in Situ Hydrolysis of Triethyl Phosphonoacetate (Crystal Growth & Design, 2006)
- Condensation of Triethyl Phosphonoacetate with Aromatic Aldehydes (Journal of Organic Chemistry, 1966)
- Alkylation of Triethyl Phosphonoacetate and Related Esters (Journal of the American Chemical Society, 1950)
- Notes- Condensation of Triethyl Phosphonoacetate with Aromatic Aldehydes (Journal of Organic Chemistry, 1960)
- A Practical Synthesis of -Keto Phosphonates from Triethyl Phosphonoacetate (Synthetic Communications, 1996)
- Preparation of Triethyl 2-Fluoro-2-phosphonoacetate (Synthetic Communications, 1994)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCCOC(=O)CP(=O)(OCC)OCC
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InChIKeyGGUBFICZYGKNTD-UHFFFAOYSA-N
- Pubchem - Triethyl phosphonoacetate
- Wikipedia - triethyl phosphonoacetate
Triethyl phosphonoacetate is a reagent for organic synthesis used in the Horner-Wadsworth-Emmons reaction (HWE) or the Horner-Emmons modification. Triethyl phosphonoacetate can be added dropwise to sodium methoxide solution to prepare a phosphonate ylide. It has an acidic proton that can easily be abstracted by a weak base.
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Triethyl phosphonoacetate
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