Weight | 132.115 g/mol |
---|---|
Formula | C5H8O4 |
Hydrogen Acceptors | 4 |
Hydrogen Donors | 0 |
Aromatic Rings | 0 |
Rotatable Bonds | 2 |
Methylene diacetate (25231-38-3, 628-51-3)
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- Organic peroxides. LXIII. Formation of di-tert-butyl polyoxides in the reaction of tert-butyl hydroperoxide with iodosobenzene and iodosobenzene diacetate in methylene chloride and in diethyl ether at -80 to +5.deg. (Journal of the American Chemical Society, 1968)
- Novel methylene modified cyclohexyl ethylenediamine-N,N'-diacetate ligands and their platinum(IV) complexes. Influence on biological activity. (Journal of Inorganic Biochemistry, 2012)
- Iodobenzene Diacetate/Tetrabutylammonium IodideInduced Aziridination of NTosylimines with Activated Methylene Compounds under Mild Conditions (Advanced Synthesis & Catalysis, 2008)
- The Hydrolysis of Methylene Diacetate and Ethylidene Diacetate in Concentrated Hydrochloric Acid Solutions. (Acta Chemica Scandinavica, 1957)
- STUDIES ON HOMOGENEOUS FIRST ORDER GAS REACTIONS: VI. THE DECOMPOSITION OF METHYLENE DIACETATE, METHYLENE DIPROPIONATE, AND METHYLENE DIBUTYRATE (Canadian journal of research, 1937)
- Substituent effect study on experimental 13C NMR chemical shifts of (3-(substituted phenyl)-cis-4,5-dihydroisoxazole-4,5-diyl)bis(methylene)diacetate derivatives (Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy, 2015)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCC(=O)OCOC(=O)C
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InChIKeyBPGDAMSIGCZZLK-UHFFFAOYSA-N
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Synthesis
Reactant
+
dimethyl sulfide
(Corey-Kim oxidation of secondary alcohols)
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