| Weight | 124.076 g/mol |
|---|---|
| Formula | C3H9O3P |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 2 |
Ethyl methylphosphonate (1832-53-7)
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- Impact of two ionic liquids, 1-ethyl-3-methylimidazolium acetate and 1-ethyl-3-methylimidazolium methylphosphonate, on Saccharomyces cerevisiae: metabolic, physiologic, and morphological investigations. (Biotechnology for Biofuels, 2015)
- The Enfrared Spectra of tris (Methyl Methylphosphonate) Iron(III), Tris (Ethyl Ethylphosphonate) Iron(III), and Tris (Isopropyl Methylphosphonate) Iron(III) (Spectroscopy Letters, 1969)
- Mechanistic studies of La3+ and Zn2+-catalyzed methanolysis of O-ethyl O-aryl methylphosphonate esters. An effective solvolytic method for the catalytic destruction of phosphonate CW simulants (Organic and Biomolecular Chemistry, 2005)
- Biotransformation and Male Rat-Specific Renal Toxicity of Diethyl Ethyl- and Dimethyl Methylphosphonate (Toxicological Sciences, 2000)
- Kinetic and mechanistic studies of the reaction of a range of bases and metal-hydroxo complexes with the phosphonate ester 2,4-dinitrophenyl ethyl methylphosphonate in aqueous solution (Transition Metal Chemistry, 1998)
- A convenient route to the phosphorus and sulfur stereoisomers of ethyl menthyl (methylsulfinyl)methylphosphonate (Tetrahedron-asymmetry, 2004)
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Predict GHS Hazards for Any Chemical in silico.
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SMILESCCOP(=O)(C)O
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InChIKeyUFZOPKFMKMAWLU-UHFFFAOYSA-N
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Similar Compounds
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diethyl hydrogen phosphate
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15110-17-5
(15110-17-5)
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7598-61-0
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6609-64-9
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(4546-04-7)
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(18733-15-8)
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(13408-09-8, 819-83-0)
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(13408-09-8, 819-83-0)
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358-63-4
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35404-71-8
(35404-71-8)
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1552-41-6
(1552-41-6)
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(757-44-8)
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(13674-84-5)
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1 alternate name
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5301-78-0
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(62778-16-9)
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88738-78-7
(88738-78-7)
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(5927-18-4)
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(53575-08-9)
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(17919-34-5)
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(1145-93-3)
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(1984-15-2, 63347-66-0)
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(822-39-9)
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(20120-33-6)
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Decylphosphonic acid
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(4724-48-5)
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Ethyl methylphosphonate
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