| Identification | More | [Name]
Dodecahydrotriphenylene | [CAS]
1610-39-5 | [Synonyms]
DODECAHYDROTRI-O-PHENYLENE
DODECAHYDROTRIPHENYLENE
1,2,3,4,5,6,7,8,9,10,11,12-Dodecahydrotriphenylene
triphenylene,1,2,3,4,5,6,7,8,9,10,11,12-dodecahydro-
Tritetralin
DODECAHYDROTRIPHENYLENE OEKANAL 250 MG | [EINECS(EC#)]
216-550-1 | [Molecular Formula]
C18H24 | [MDL Number]
MFCD00001109 | [Molecular Weight]
240.38 | [MOL File]
1610-39-5.mol |
| Chemical Properties | Back Directory | [Appearance]
white to yellow-beige fine crystalline powder | [Melting point ]
231-233 °C (lit.) | [Boiling point ]
318.11°C (rough estimate) | [density ]
0.9356 (estimate) | [refractive index ]
1.5500 (estimate) | [solubility ]
hexane: soluble | [form ]
solid | [BRN ]
2051002 | [CAS DataBase Reference]
1610-39-5(CAS DataBase Reference) | [NIST Chemistry Reference]
Triphenylene, 1,2,3,4,5,6,7,8,9,10,11,12-dodecahydro-(1610-39-5) |
| Hazard Information | Back Directory | [Chemical Properties]
white to yellow-beige fine crystalline powder | [Uses]
Dodecahydrotriphenylene was used to develop a set of new bacterial bioreporters and assays for detection of long chain alkanes based on the marine bacterium Alcanivorax borkumensis strain SK2. | [General Description]
Dodecahydrotriphenylene forms metal-carbonyl complexes. It undergoes hydrogenation and rearrangement by action of AlCl3 in inert atmosphere conditions at 20°C (hexane solution) or 70°C (heptane solution). It is formed by trimerization of cyclohexanone. It undergoes oxidation by peroxytrifluoroacetic acid and boron fluoride etherate at 0°C to form cross-conjugated cyclohexadieone. |
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