Weight | 142.154 g/mol |
---|---|
Formula | C7H10O3 |
Hydrogen Acceptors | 3 |
Hydrogen Donors | 0 |
Aromatic Rings | 0 |
Rotatable Bonds | 0 |
2,2,6-Trimethyl-4H-1,3-dioxin-4-one (5394-63-8)
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- Acetoacetylation with 2,2,6-trimethyl-4H-1,3-dioxin-4-one: a convenient alternative to diketene (Journal of Organic Chemistry, 1985)
- Ketenes. 20. Thermal decomposition of 2,2,6-trimethyl-4H-1,3-dioxin-4-one and 1-ethoxybutyn-3-one. Acetylketene (Journal of Organic Chemistry, 1984)
- Kinetic and spectroscopic studies on the thermal decomposition of 2,2,6-trimethyl-4H-1,3-dioxin-4-one. Generation of acetylketene (Journal of the American Chemical Society, 1989)
- FLASH PHOTOLYSIS OF 2,2,6-TRIMETHYL-4H-1,3-DIOXIN-4-ONE IN AQUEOUS SOLUTION : HYDRATION OF ACETYLKETENE AND KETONIZATION OF ACETOACETIC ACID ENOL (Journal of the American Chemical Society, 1996)
- Reaction of 2,2,6-trimethyl-4H-1,3-dioxin-4-one with imines: an easy route to enamides (Tetrahedron Letters, 1996)
- A Computational Study of the Thermal Cycloreversion of 2,2,6-Trimethyl-4H-1,3-dioxin-4-one and a Related Species: Retro-Diels-Alder Reaction or Concerted Nucleophilic Attack? (Journal of Organic Chemistry, 1995)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCC1=CC(=O)OC(O1)(C)C
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InChIKeyXFRBXZCBOYNMJP-UHFFFAOYSA-N
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