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Names | |
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Preferred IUPAC name
(Hexan-2-yl)benzene | |
Other names
2-Phenylhexane
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Identifiers | |
3D model (
JSmol)
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ChemSpider | |
PubChem
CID
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UNII | |
CompTox Dashboard (
EPA)
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Properties | |
C12H18 | |
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).
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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]
![]() | |
Names | |
---|---|
Preferred IUPAC name
(Hexan-2-yl)benzene | |
Other names
2-Phenylhexane
| |
Identifiers | |
3D model (
JSmol)
|
|
ChemSpider | |
PubChem
CID
|
|
UNII | |
CompTox Dashboard (
EPA)
|
|
| |
| |
Properties | |
C12H18 | |
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).
|
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]