Weight | 130.187 g/mol |
---|---|
Formula | C7H14O2 |
Hydrogen Acceptors | 2 |
Hydrogen Donors | 0 |
Aromatic Rings | 0 |
Rotatable Bonds | 1 |
Ethyl trimethylacetate (3938-95-2)
ethyl pivalate
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- Syntheses and Magnetic Properties of Ruthenium(II,III) Pivalate Dimers Axially Coordinated by Nitronyl Nitroxide Radicals [Ru2(O2CCMe3)4(L)2]BF4and [{Ru2(O2CCMe3)4(L)2}{Ru2(O2CCMe3)4(H2O)2}]n(BF4)2n, L = 2,4,4,5,5-Pentamethyl-4,5-dihydro-1H-imidazol-1-oxyl-3-N-oxide and 2-Ethyl-4,4,5,5-tetramethyl-4,5-dihydro-1H-imidazol-1-oxyl-3-N-oxide (Bulletin of the Chemical Society of Japan, 2003)
- Two conformers of ethyl pivalate studied by microwave spectroscopy (Journal of Molecular Spectroscopy, 2010)
- Solubility Behavior of Phenolic Compounds in Hexaneethyl Acetate, Hexaneethyl Myristate, and Hexane-Ethyl Pivalate Cosolvent Systems (Journal of Pharmaceutical Sciences, 1981)
- Reaction or ethyl diazoacetate with halogenoethylenes in the presence of rhodium(II) pivalate (Journal of Organometallic Chemistry, 1984)
- The thermal decomposition of ethyl trimethylacetate (Australian Journal of Chemistry, 1967)
- The preparation of ethyl and isopropyl dienol ethers and dienol pivalate esters from Hagemann's ester and its t-butyl analogue, and the reactions of the derived ester dienolates with electrophiles (Australian Journal of Chemistry, 1984)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - ethyl pivalate
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SMILESCCOC(=O)C(C)(C)C
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InChIKeyHHEIMYAXCOIQCJ-UHFFFAOYSA-N
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Synthesis
Reactant
+
dimethyl sulfide
(Corey-Kim oxidation of secondary alcohols)
Similar Compounds
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