2-Phenylhexane
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| 2-Phenylhexane | |
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| IUPAC name | Hexan-2-ylbenzene, |
| Other names | 2-Phenylhexane |
| Identifiers | |
| CAS number | [6031-02-3] |
| PubChem | |
| SMILES | CCCCC(C)C1=CC=CC=C1 |
| InChI | InChI=1/C12H18/c1-3-4-8-11(2)12-9-6-5-7-10-12/h5-7,9-11H,3-4,8H2,1-2H3 |
| Properties | |
| Molecular formula | C12H18 |
| Molar mass | 162.27 g/mol |
| Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa) Infobox disclaimer and references |
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2-Phenylhexane is an aromatic hydrocarbon. It can be produced by a Friedel-Crafts alkylation between 1-chlorohexane and benzene.[1], or by the reaction of benzene and 1-hexene with various acid catalysts such as antimony pentafluoride,[2] scandium(III) triflate,[3] and phosphoric acid.[4]
[edit] References
- ^ Organic Chemistry Marye Anne Fox, James K. Whitesell (Google books)
- ^ Zhurnal Organicheskoi Khimii, 17(7), 1505-11; 1981
- ^ Choong Eui Song; Woo Ho Shimb; Eun Joo Roha; Jung Hoon Choi (2000). "Scandium(III) triflate immobilised in ionic liquids: a novel and recyclable catalytic system for FriedelCrafts alkylation of aromatic compounds with alkenes". Chem. Commun. 2000 (17): 1695–1696. doi:.
- ^ Industrial & Engineering Chemistry Research, 46(9), 2902-2906; 2007
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