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Ethyl-2-(diethylphosphono)propanoate

Catalog Number
ACM3699669
Product Name
Ethyl-2-(diethylphosphono)propanoate
Structure
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CAS
3699-66-9
  • Product Overview
  • Usage
Synonyms
Triethyl 2-phosphonopropionate; 2-(Diethoxyphosphoryl)propionic acid ethyl ester
IUPAC Name
ethyl 2-diethoxyphosphorylpropanoate
Molecular Weight
238.22
Molecular Formula
C9H19O5P
Canonical SMILES
CCOC(=O)C(C)P(=O)(OCC)OCC;
InChI
BVSRWCMAJISCTD-UHFFFAOYSA-N
InChI Key
InChI=1S/C9H19O5P/c1-5-12-9(10)8(4)15(11,13-6-2)14-7-3/h8H,5-7H2,1-4H3
Boiling Point
143-144 °C at 12 mmHg(lit.)
Flash Point
192 °F
Purity
98%
Density
1.111 g/mL at 25 °C(lit.)
Appearance
Liquid
Storage
-20°C
Complexity
231
Covalently-Bonded Unit Count
1
EC Number
223-033-4
Exact Mass
238.097g/mol
H-Bond Acceptor
5
Heavy Atom Count
15
Isomeric SMILES
CCOC(=O)C(C)P(=O)(OCC)OCC
Monoisotopic Mass
238.097g/mol
NSC Number
202767
Rotatable Bond Count
8
Topological Polar Surface Area
61.8A^2
Undefined Atom Stereocenter Count
1
Application
Ethyl-2-(diethylphosphono)propanoate is a versatile compound utilized in various chemical and biological applications. It is a crucial component in research on insecticides, exploring their effectiveness against different bacteria, and acts as an inhibitor for the transmission and infection of the Epstein-Barr virus. In synthetic chemistry, this compound serves as a reactant in intramolecular conjugate additions, facilitating the synthesis of complex molecules such as floresolide B and spiroindane di-methyl acetic acid, while also participating in stereoselective intramolecular Diels-Alder reactions. Furthermore, it plays a significant role in Horner-Wadsworth-Emmons reactions, as well as in the chemoenzymatic one-pot synthesis of gamma-butyrolactones. Additionally, Ethyl-2-(diethylphosphono)propanoate is employed in synthesizing compounds like 3-[2]furyl-2-methyl-acrylic acid ethyl ester through reactions with furfural. This clear, colorless liquid proves essential in advancing both pharmaceutical and synthetic methodologies.
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