Weight | 102.089 g/mol |
---|---|
Formula | C4H6O3 |
Hydrogen Acceptors | 3 |
Hydrogen Donors | 0 |
Aromatic Rings | 0 |
Rotatable Bonds | 0 |
1,3-Dioxan-2-one (2453-03-4, 31852-84-3)
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- Novel functional polycarbonate by lipase-catalyzed ring-opening polymerization of 5-methyl-5-benzyloxycarbonyl-1,3-dioxan-2-one (Macromolecules, 1999)
- Synthesis of copolymers of 1,3-dioxan-2-one and oxepan-2-one using coordination catalysts (Journal of Polymer Science Part A, 1994)
- Enzyme-Catalyzed Ring-Opening Polymerization of 1,3-Dioxan-2-one to Poly(trimethylene carbonate) (Macromolecules, 1997)
- Enzyme-catalyzed ring-opening copolymerization of 5-methyl-5-benzyloxycarbonyl-1,3-dioxan-2-one (MBC) with trimethylene carbonate (TMC): synthesis and characterization. (Biomacromolecules, 2000)
- New aliphatic poly(estercarbonates) based on 5methyl5allyloxycarbonyl1,3dioxan2one (Journal of Polymer Science Part A, 2003)
- Lipase-catalyzed ring-opening polymerization of 1,3-dioxan-2-one (Macromolecular Rapid Communications, 1997)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1COC(=O)OC1
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InChIKeyYFHICDDUDORKJB-UHFFFAOYSA-N
- Pubchem - 1,3-Dioxan-2-one
- Wikipedia - trimethylene carbonate
Trimethylene carbonate or 1,3-propylene carbonate is a 6-membered cyclic carbonate ester. It is a colourless solid that upon heating or catalytic ring-opening converts to the poly(trimethylene carbonate). Such polymers are called aliphatic polycarbonates are of interest for potential biomedical applications.
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Similar Compounds
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5-Methyl-5-propyl-1,3-dioxan-2-one
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diethyl pyrocarbonate
(1609-47-8)
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(628-66-0)
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(2544-06-1, 38094-42-7)
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(7789-92-6)
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ethyl 3-hydroxypropanoate
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(629-33-4)
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