- 2-Phenylhexane
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2-Phenylhexane 
Hexan-2-ylbenzene,Other names2-PhenylhexaneIdentifiers CAS number 6031-02-3 PubChem 22385 ChemSpider 21010 
Jmol-3D images Image 1
Image 2- CCCCC(C)C1=CC=CC=C1
c1ccccc1C(CCCC)C
- InChI=1S/C12H18/c1-3-4-8-11(2)12-9-6-5-7-10-12/h5-7,9-11H,3-4,8H2,1-2H3
Key: CYBSWFUWEZFKNJ-UHFFFAOYSA-NInChI=1/C12H18/c1-3-4-8-11(2)12-9-6-5-7-10-12/h5-7,9-11H,3-4,8H2,1-2H3
Key: CYBSWFUWEZFKNJ-UHFFFAOYAV
Properties Molecular formula C12H18 Molar mass 162.27 g/mol 
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Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa)Infobox references 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]
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 Friedel-Crafts alkylation of aromatic compounds with alkenes". Chem. Commun. 2000 (17): 1695–1696. doi:10.1039/b005335j.
- ^ Industrial & Engineering Chemistry Research, 46(9), 2902-2906; 2007
Alkanes • Alkenes • Alkynes • Cycloalkanes • Cycloalkenes • Cycloalkynes • Arenes (Aromatic hydrocarbons)
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