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CAS RN: 682-30-4 | Product Number: D3728
Diethyl Vinylphosphonate
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Purity: >98.0%(GC)
Synonyms:
- Vinylphosphonic Acid Diethyl Ester
Product Documents:
| Size | Unit Price | Saitama (Kawaguchi) | Hyogo (Amagasaki) | Stock in other WH |
Shipping Information
|
|---|---|---|---|---|---|
| 5G |
¥9,900
|
18 | 14 | ≥100 |
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* The displayed price is the unit price and does not include consumption tax. The unit prices displayed are the latest and are subject to change without notice.
* To send your quote request for bulk quantities, please click on the "Request Bulk Quote" button. Please note that we cannot offer bulk quantities for some products.
*TCI frequently reviews storage conditions to optimize them. Please note that the latest information on the storage temperature for the products is described on our website.
| Product Number | D3728 |
Purity / Analysis Method 
|
>98.0%(GC) |
| Molecular Formula / Molecular Weight | C__6H__1__3O__3P = 164.14 |
| Physical State (20 deg.C) | Liquid |
| Storage Temperature
|
Refrigerated (0-10°C) |
| Condition to Avoid | Heat Sensitive |
| CAS RN | 682-30-4 |
| Reaxys Registry Number | 507596 |
| PubChem Substance ID | 87560563 |
| MDL Number | MFCD00009079 |
Specifications
| Appearance | Colorless to Almost colorless clear liquid |
| Purity(GC) | min. 98.0 % |
Properties (reference)
| Boiling Point | 82 °C/15 mmHg |
| Specific Gravity (20/20) | 1.06 |
| Refractive Index | 1.43 |
GHS
Related Laws:
| Fire Defense Law | Group-4-3-III |
| RTECS# | TA1150000 |
Transport Information:
Application
A Stereoselective synthesis of Z-Enamides
Experimental procedure1): to a dry flask is charged with amide (0.35 mmol), PdCl2(PhCN)2 (0.017 mmol), and CuCl (0.035 mmol). The reaction vessel is charged with oxygen followed by the addition of chlorobenzene (2 mL) and tetraethyl methylenediphosphonate (TEMDP, 0.035 mmol). The reaction mixture is stirred at 70 °C for 1 min and then diethyl vinylphosphonate (1.05 mmol) is added. The reaction mixture is stirred at 70 °C for 48 h under oxygen atmosphere. After the reaction is over, the solvent is evaporated under reduced pressure and the crude residue is purified by flash column chromatograph.
References
- 1) Hydrogen-Bond-Directed Highly Stereoselective Synthesis of Z-Enamides via Pd-Catalyzed Oxidative Amidation of Conjugated Olefins
- 2) Pd(II)-Catalyzed Hydroxyl-Directed C-H Olefination Enabled by Monoprotected Amino Acid Ligands
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