Chemistry:1,1,1-Trichloroacetone
From HandWiki
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| Names | |
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| Preferred IUPAC name
1,1,1-Trichloropropan-2-one | |
| Other names
1,1,1-Trichloroacetone
1,1,1-Trichloropropanone | |
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3D model (JSmol)
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| Properties | |
| C3H3Cl3O | |
| Molar mass | 161.41 g·mol−1 |
| Appearance | Colourless liquid |
| Density | 1.475 g/cm3 |
| Boiling point | 134 °C (273 °F; 407 K)[1] |
| slightly soluble | |
| Solubility | Soluble in ethanol and diethyl ether |
| Hazards | |
| Main hazards | Irritant |
| GHS pictograms | 
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| GHS Signal word | Warning |
| H315, H319, H335 | |
| P261, P264, P271, P280, P302+352, P304+340, P305+351+338, P312, P321, P332+313, P337+313, P362, P403+233, P405, P501 | |
| Flash point | 64 °C (147 °F; 337 K) |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
| Infobox references | |
1,1,1-Trichloroacetone is a chlorinated analogue of acetone with the chemical formula CH3COCCl3. It is a colourless liquid. 1,1,1-Trichloroacetone can be synthesised from chlorination of chloroacetone (1,1,3-trichloroacetone is formed as a by-product). An alternative synthesis involves the transfer of a trichloromethyl group from trichloroacetate onto acetyl chloride.[2]
See also
- Chloroacetone
- 1,3-Dichloroacetone
- Hexachloroacetone
References
- ↑ "1,1,1-TRICHLOROACETONE CAS#: 918-00-3". https://m.chemicalbook.com/ProductChemicalPropertiesCB9175765_EN.htm.
- ↑ Taschner, Michael J. (2001). "Sodium Trichloroacetate". e-EROS Encyclopedia of Reagents for Organic Synthesis. doi:10.1002/047084289X.rs113. ISBN 0471936235.
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