| Identification | Back Directory | [Name]
DIETHYL-3-BUTENYLPHOSPHONATE 95 | [CAS]
15916-48-0 | [Synonyms]
SKL409
Diethyl 3-butenylphosphonate 95%
DIETHYL-3-BUTENYLPHOSPHONATE 95
diethyl but-3-en-1-ylphosphonate
P-3-Buten-1-yl-phosphonic acid diethyl ester
Phosphonic acid, P-3-buten-1-yl-, diethyl ester | [Molecular Formula]
C8H17O3P | [MDL Number]
MFCD06200726 | [MOL File]
15916-48-0.mol | [Molecular Weight]
192.19 |
| Chemical Properties | Back Directory | [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 |
| Safety Data | Back Directory | [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 |
| Hazard Information | Back Directory | [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 |
|
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Energy Chemical
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http://www.energy-chemical.com |
| Company Name: |
Sigma-Aldrich
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https://www.sigmaaldrich.cn |
| Company Name: |
Merck KGaA
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www.sigmaaldrich.cn |
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