From Wikipedia, the free encyclopedia
2-Phenylhexane
Names
Preferred IUPAC name
Other names
2-Phenylhexane
Identifiers
ChemSpider
UNII
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
CCCCC(C)C1=CC=CC=C1
c1ccccc1C(CCCC)C
Properties
C 12 H 18
Molar mass
162.276 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).
Chemical compound
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