| Company Name: |
Energy Chemical |
| Tel: |
400-0056266 |
| Email: |
sales8178@energy-chemical.com |
| Company Name: |
Sigma-Aldrich |
| Tel: |
021-61415566 800-8193336 |
| Email: |
orderCN@merckgroup.com |
|
| | Diethyl-3-butenylphosphonate 95 Basic information |
| | Diethyl-3-butenylphosphonate 95 Chemical Properties |
| Boiling point | 55 °C/0.55 mmHg (lit.) | | density | 1.005 g/mL at 25 °C (lit.) | | Fp | 222 °F | | InChI | 1S/C8H17O3P/c1-4-7-8-12(9,10-5-2)11-6-3/h4H,1,5-8H2,2-3H3 | | InChIKey | NUDGAPYPOAQVLP-UHFFFAOYSA-N | | SMILES | CCOP(=O)(CCC=C)OCC |
| Hazard Codes | T | | Risk Statements | 25 | | Safety Statements | 45 | | RIDADR | UN 2810 6.1/PG 3 | | WGK Germany | 3 | | Storage Class | 6.1C - Combustible acute toxic Cat.3
toxic compounds or compounds which causing chronic effects | | Hazard Classifications | Acute Tox. 3 Oral |
| | Diethyl-3-butenylphosphonate 95 Usage And Synthesis |
| Uses | Reactant for synthesis of:
- Bicyclo[3.3.1]alkenone framework compounds by gold-catalyzed Diels-Alder reactions
- Antiviral C-5-substituted pyrimidine acyclic nucleoside phosphonates selected as human thymidylate kinase substrates
- Antimalarials via halogenation of di-Et butenylphosphonate
- Bisphosphonate enynes
Reactant for:
- Remote supramolecular control of catalyst selectivity in hydroformlyation of alkenes
- Intermolecular metal-catalyzed carbenoid cyclopropanations
- Chemoenzymatic synthesis of phosphic derivatives of carbohydrates
| | reaction suitability | reaction type: C-C Bond Formation |
| | Diethyl-3-butenylphosphonate 95 Preparation Products And Raw materials |
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