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Names | |
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IUPAC name
Tricyclo[8.2.2.24,7]hexadeca-4,6,10,12,13,15-hexaene
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Other names
[2.2](1,4)Cyclophane
1,4-Carbophane Cyclobis(benzene-1,4-dimethylene) Parylene dimer Di-p-xylylene | |
Identifiers | |
3D model (
JSmol)
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ChEMBL | |
ChemSpider | |
ECHA InfoCard | 100.015.132 |
EC Number |
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PubChem
CID
|
|
CompTox Dashboard (
EPA)
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|
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Properties | |
C16H16 | |
Molar mass | 208.304 g·mol−1 |
Appearance | White solid [1] |
Density | 1.242 g/cm3 (260 K) [2] |
Melting point | 285 °C (545 °F; 558 K) [3] |
Hazards | |
GHS labelling: [4] | |
![]() ![]() | |
Warning | |
H317, H373 | |
P260, P261, P272, P280, P302+P352, P319, P321, P333+P317, P362+P364, P501 | |
Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
|
[2.2]Paracyclophane is a cyclophane that is applied in bio- and materials science. It was first synthesized by Brown and Farthing in 1949 by pyrolyzing para-xylene in the gas phase under low pressure. [3]
[2.2]Paracyclophane is stable under normal conditions. Its formyl, acetyl, nitro- and bromo- derivatives can be obtained by electrophilic aromatic substitution in one step. [5]
![]() | |
Names | |
---|---|
IUPAC name
Tricyclo[8.2.2.24,7]hexadeca-4,6,10,12,13,15-hexaene
| |
Other names
[2.2](1,4)Cyclophane
1,4-Carbophane Cyclobis(benzene-1,4-dimethylene) Parylene dimer Di-p-xylylene | |
Identifiers | |
3D model (
JSmol)
|
|
ChEMBL | |
ChemSpider | |
ECHA InfoCard | 100.015.132 |
EC Number |
|
PubChem
CID
|
|
CompTox Dashboard (
EPA)
|
|
| |
Properties | |
C16H16 | |
Molar mass | 208.304 g·mol−1 |
Appearance | White solid [1] |
Density | 1.242 g/cm3 (260 K) [2] |
Melting point | 285 °C (545 °F; 558 K) [3] |
Hazards | |
GHS labelling: [4] | |
![]() ![]() | |
Warning | |
H317, H373 | |
P260, P261, P272, P280, P302+P352, P319, P321, P333+P317, P362+P364, P501 | |
Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
|
[2.2]Paracyclophane is a cyclophane that is applied in bio- and materials science. It was first synthesized by Brown and Farthing in 1949 by pyrolyzing para-xylene in the gas phase under low pressure. [3]
[2.2]Paracyclophane is stable under normal conditions. Its formyl, acetyl, nitro- and bromo- derivatives can be obtained by electrophilic aromatic substitution in one step. [5]