174653
Triethyl 2-phosphonopropionate
98%
Synonym(s):
2-(Diethoxyphosphoryl)propionic acid ethyl ester
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About This Item
Linear Formula:
(C2H5O)2P(O)CH(CH3)CO2C2H5
CAS Number:
Molecular Weight:
238.22
UNSPSC Code:
12352108
NACRES:
NA.22
PubChem Substance ID:
EC Number:
223-033-4
Beilstein/REAXYS Number:
1786994
MDL number:
Assay:
98%
Form:
liquid
InChI key
BVSRWCMAJISCTD-UHFFFAOYSA-N
InChI
1S/C9H19O5P/c1-5-12-9(10)8(4)15(11,13-6-2)14-7-3/h8H,5-7H2,1-4H3
SMILES string
CCOC(=O)C(C)P(=O)(OCC)OCC
assay
98%
form
liquid
reaction suitability
reaction type: C-C Bond Formation
Quality Level
bp
143-144 °C/12 mmHg (lit.)
density
1.111 g/mL at 25 °C (lit.)
functional group
ester, phosphonate
Related Categories
Application
Reactant involved in:
- Intramolecular conjugate addition for the synthesis of floresolide B
- Chemoenzymatic one-pot synthesis of γ-butyrolactones
- Enantioselective synthesis of spiroindane di-Me acetic acid via asymmetric hydrogenation
- Stereoselective intramolecular Diels-Alder reactions
- Horner-Wadsworth-Emmons reactions
This Wittig-Horner reagent condenses with a wide variety of aldehydes and ketones to form acrylates.
Storage Class
10 - Combustible liquids
wgk
WGK 3
flash_point_f
192.2 °F - closed cup
flash_point_c
89 °C - closed cup
ppe
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
Regulatory Information
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Find documentation for the products that you have recently purchased in the Document Library.
Tetrahedron, 48, 10327-10327 (1992)
Synthetic Communications, 21, 17-17 (1991)
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