| Weight | 288.217 g/mol |
|---|---|
| Formula | C9H22O6P2 |
| Hydrogen Acceptors | 6 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 10 |
Tetraethyl methylenediphosphonate (1660-94-2)
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- Synthesis of Carboxylic Acids via POActivated Olefination of Tetraethyl Dimethylaminomethylenediphosphonate (Angewandte Chemie, 1968)
- A Cheap One-Pot Approach to Tetraethyl Methylenediphosphonate (Synthetic Communications, 1990)
- DRY REACTION OF DIETHYL CYANOMETHYLPHOSPHONATE AND TETRAETHYL METHYLENEDIPHOSPHONATE WITH BENZALDEHYDE ON SOLID BASES (Phosphorus Sulfur and Silicon and The Related Elements, 1996)
- The structure and spectroscopic characterization of complexes with tetraethyl methylenediphosphonate in solution and in solid state (Journal of Molecular Structure, 2012)
- Reaction of [70]Fullerene with Tetraethyl Methylenediphosphonate or Diethyl (Cyanomethyl)phosphonate Revisited (European Journal of Organic Chemistry, 2010)
- Kinetics of hydrolysis of tetraethyl-methylenediphosphonate (Russian Chemical Bulletin, 1968)
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Predict GHS Hazards for Any Chemical in silico.
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SMILESCCOP(=O)(CP(=O)(OCC)OCC)OCC
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InChIKeySTJWVOQLJPNAQL-UHFFFAOYSA-N
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Tetraethyl methylenediphosphonate
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