1,3,5-Triethylbenzene
1,3,5-Triethylbenzene is a chemical compound of the group of aromatic hydrocarbons.
Names | |
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IUPAC name
1,3,5-Triethylbenzene | |
Systematic IUPAC name
yes | |
Other names
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Identifiers | |
3D model (JSmol) |
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ECHA InfoCard | 100.002.744 |
EC Number |
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MeSH | 1,3,5-triethylbenzene |
PubChem CID |
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UNII | |
CompTox Dashboard (EPA) |
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Properties | |
C12H18 | |
Molar mass | 162.27 g·mol−1 |
Appearance | colorless liquid [1] |
Density | 0.862 g·cm−3[1] |
Melting point | −66.5 °C (−87.7 °F; 206.7 K)[2] |
Boiling point | 215 °C (419 °F; 488 K)[1] |
practically insoluble [1] | |
Solubility in ethanol, diethyl ether | soluble[3] |
Hazards | |
Safety data sheet | [1] |
GHS pictograms | |
GHS Signal word | Warning |
GHS hazard statements |
H315, H319, H413 |
P305+351+338 | |
Flash point | 76 °C[1] |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
Infobox references | |
Preparation
1,3,5-Triethylbenzene can be prepared by a Friedel-Crafts alkylation of benzene with ethyl bromide in presence of aluminum chloride.[4]
Properties
1,3,5-Triethylbenzene is a flammable, hard to ignite, colorless liquid that is almost insoluble in water.[1] The refractive index is 1.495[5]
Uses
1,3,5-Triethylbenzene can be used in synthesis of a series of di- and trinucleating ligands.[5]
Safety notes
The vapour of 1,3,5-Triethylbenzene can form an explosive mixture with air (flash point: 76 °C).[1]
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References
- Record of 1,3,5-Triethylbenzol in the GESTIS Substance Database of the Institute for Occupational Safety and Health, accessed on 15 March 2019.
- David R. Lide (1995). CRC Handbook of Chemistry and Physics A Ready-reference Book of Chemical and Physical Data. CRC Press. p. 544. ISBN 978-0-8493-0595-5.
- "1,3,5-Triethylbenzene, 95%". Alfa Aesar. Retrieved 15 March 2019.
- Stanley R. Sandler, Wolf Karo (2012). Sourcebook of Advanced Organic Laboratory Preparations. Academic Press. p. 12. ISBN 0-08-092553-7.
- Sigma-Aldrich Co., 1,3,5-Triethylbenzene, ≥97%. Retrieved on 15 March 2019.
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