2-Phenylhexane

2-Phenylhexane

Names
IUPAC name Hexan-2-ylbenzene
Other names 2-Phenylhexane
Identifiers
CAS Number	6031-02-3 N
3D model (Jmol)	Interactive image Interactive image
ChemSpider	21010 Y
PubChem	22385
UNII	8I5F5V031E N
InChI 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 Y Key: CYBSWFUWEZFKNJ-UHFFFAOYSA-N Y 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 Key: CYBSWFUWEZFKNJ-UHFFFAOYAV
SMILES CCCCC(C)C1=CC=CC=C1 c1ccccc1C(CCCC)C
Properties
Chemical formula	C12H18
Molar mass	162.28 g·mol−1
Density	0.858 g/ml
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
N verify (what is YN ?)
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

1. ↑ Organic Chemistry Marye Anne Fox, James K. Whitesell (Google books)
2. ↑ Zhurnal Organicheskoi Khimii, 17(7), 1505-11; 1981
3. ↑ 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. 
4. ↑ Industrial & Engineering Chemistry Research, 46(9), 2902-2906; 2007