Oxazolidine
Encyclopedia : O : OX : OXA : Oxazolidine
| Oxazolidine | |
|---|---|
|
| |
| General | |
| Systematic name | oxazolidine |
| Other names | 1,3-oxazolidine |
| Molecular formula | C3H7NO |
| SMILES | C1COCN1 |
| Molar mass | 73.0938 g/mol |
| Appearance | ? |
| CAS number | [504-76-7] |
| Properties | |
| Density and phase | ? g/cm3, ? |
| Solubility in water | ? g/100 ml (? °C) |
| Melting point | ? °C (? K) |
| Boiling point | ? °C (? K) |
| Acidity (pKa) | ? |
| Basicity (pKb) | ? |
| Chiral rotation | ?° |
| Viscosity | ? cP at ? °C |
| Structure | |
| Molecular shape | ? |
| Coordination geometry | ? |
| Crystal structure | ? |
| Dipole moment | ? D |
| Hazards | |
| MSDS | External MSDS |
| Main hazards | ? |
| NFPA 704 | |
| Flash point | ? °C |
| R/S statement | R: ? S: ? |
| RTECS number | ? |
| Supplementary data page | |
| Structure and properties | n, εr, etc. |
| Thermodynamic data | Phase behaviour Solid, liquid, gas |
| Spectral data | UV, IR, NMR, MS |
| Related compounds | |
| Other anions | ? |
| Other cations | ? |
| Related ? | ? |
| Related compounds | ? |
| Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa) [Chemical infoboxInfobox disclaimer and references] | |
Bisoxazolidines
Bisoxazolidines have two oxazolidine rings, and they are used as reactive diluents in polyurethane paints. The rings hydrolyze in the presence of moisture into amine and hydroxyl groups, which can then bind with diisocyanates to form the coating.[#endnote_paint]See also
- Azole
- Isoxazole, an analog with the nitrogen atom in position 2.
- Imidazole, an analog with the oxygen replaced by a nitrogen.
- Thiazole, an analog with the oxygen replaced by a sulfur.
- Benzoxazole, where the oxazole is fused to another aromatic ring.
- Pyrrole, an analog without the oxygen atom.
- Furan, an analog without the nitrogen atom.
- Oxazoline, which has only one double bond reduced.
- Oxazolidinedione, which has two in-cycle keto groups (a carbamate and a lactam).
- Oxazolidinone, which has an in-cycle carbamate.
- Simple aromatic rings
References and End Notes
- ↑ Dr Neil G Carter [OXAZOLIDINE DILUENTS : REACTING FOR THE ENVIRONMENT] Industrial Copolymers Limited
- ↑ [Emission control] chembytes e-zine 2001.
External links
- For a full list of external links to MSDSs, spectroscopic data, commercial chemicals suppliers etc. for this compound, see [Chemical sources].
From Wikipedia, the Free Encyclopedia. Original article here. Support Wikipedia by contributing or donating.
All text is available under the terms of the GNU Free Documentation License See Wikipedia Copyrights for details.