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化驗
99%
形狀
solid
mp
231-233 °C (lit.)
溶解度
hexane: soluble
SMILES 字串
C1CCc2c(C1)c3CCCCc3c4CCCCc24
InChI
1S/C18H24/c1-2-8-14-13(7-1)15-9-3-4-11-17(15)18-12-6-5-10-16(14)18/h1-12H2
InChI 密鑰
ODHYDPYRIQKHCI-UHFFFAOYSA-N
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一般說明
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.
應用
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.
儲存類別代碼
11 - Combustible Solids
水污染物質分類（WGK）
WGK 3
閃點（°F）
Not applicable
閃點（°C）
Not applicable
個人防護裝備
Eyeshields, Gloves, type N95 (US)
Oxidations with peroxytrifluoracetic acid-boron fluoride. X. Oxidation of s-dodecahydrotriphenylene with peroxytrifluoracetic acid-boron fluoride and the photoisomerization of the resulting cyclohexadienones.
Hart H and Lankin DC.
The Journal of Organic Chemistry, 33(12), 4398-4402 (1968)
Metal-carbonyl complexes of dodecahydrotriphenylene; a comparison of the structures of iso-electronic [(η6C18H24) Mn (CO)3]+ and (η6C18H24) Cr (CO)3.
Gommans LHP, et al.
Journal of Organometallic Chemistry, 346(3), 385-395 (1988)
Hydrogenation and rearrangement of coal-related aromatic and hydroaromatic molecules promoted under mild conditions by aluminium trichloride.
Stobart SR and Zaworotko MJ.
Fuel: The Science and Technology of Fuel and Energy, 64(11), 1623-1624 (1985)
Rekha Kumari et al.
Environmental microbiology, 13(10), 2808-2819 (2011-09-08)
Long-chain alkanes are a major component of crude oil and therefore potentially good indicators of hydrocarbon spills. Here we present a set of new bacterial bioreporters and assays that allow to detect long-chain alkanes. These reporters are based on the
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