2-Phenylhexane
Names | |
---|---|
Preferred IUPAC name (Hexan-2-yl)benzene | |
Other names 2-Phenylhexane | |
Identifiers | |
CAS Number |
|
3D model (JSmol) |
|
ChemSpider |
|
PubChem CID |
|
UNII |
|
CompTox Dashboard (EPA) |
|
InChI
| |
| |
Properties | |
Chemical formula | 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). N verify (what is YN ?) Infobox references |
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
- v
- t
- e
aliphatic
hydrocarbons
Alkanes CnH2n + 2 |
| ||||
---|---|---|---|---|---|
Cycloalkanes | |||||
Alkylcycloalkanes |
| ||||
Bicycloalkanes |
| ||||
Polycycloalkanes |
| ||||
Other |
|
aliphatic
hydrocarbons
Alkenes CnH2n |
| ||||
---|---|---|---|---|---|
Alkynes CnH2n − 2 |
| ||||
Cycloalkenes | |||||
Alkylcycloalkenes |
| ||||
Bicycloalkenes | |||||
Cycloalkynes |
| ||||
Dienes |
| ||||
Other |
|
hydrocarbons
PAHs |
| ||||||||||||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Alkylbenzenes |
| ||||||||||||||||||||||
Vinylbenzenes | |||||||||||||||||||||||
Other |
|
This article about a hydrocarbon is a stub. You can help Wikipedia by expanding it. |
- v
- t
- e
This article about an aromatic compound is a stub. You can help Wikipedia by expanding it. |
- v
- t
- e