perhydroacenaphthene

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Products Intro: Product Name:perhydroacenaphthene
CAS:2146-36-3
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Products Intro: CAS:2146-36-3
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Products Intro: Product Name:perhydroacenaphthene
CAS:2146-36-3
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CAS:2146-36-3
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Products Intro: Product Name:perhydroacenaphthene
CAS:2146-36-3

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perhydroacenaphthene Basic information
Product Name:perhydroacenaphthene
Synonyms:Perhydroacenaphthene 2146-36-3 Decahydroacenaphthene;perhydroacephthene;perhydroacenaphthene;Decahydroacenaphthene;Tricyclo(6,3,1,04,12)dodecane;Dodecahydroacenaphthylene;Tricyclo[7.2.1.05,12]dodecane;Acenaphthylene, dodecahydro-
CAS:2146-36-3
MF:C12H20
MW:164.29
EINECS:218-412-6
Product Categories:
Mol File:2146-36-3.mol
perhydroacenaphthene Structure
perhydroacenaphthene Chemical Properties
Melting point 36℃
Boiling point 235℃
density 1.029 g/cm3
refractive index 1.577 (589.3 nm 20℃)
storage temp. 2-8°C
form Liquid
color Yellowish brown
InChIInChI=1S/C12H20/c1-3-9-4-2-6-11-8-7-10(5-1)12(9)11/h9-12H,1-8H2
InChIKeyFZDZWLDRELLWNN-UHFFFAOYSA-N
SMILESC1C2C3C(CCC2)CCCC3C1
EPA Substance Registry SystemAcenaphthylene, dodecahydro- (2146-36-3)
Safety Information
TSCA TSCA listed
MSDS Information
perhydroacenaphthene Usage And Synthesis
UsesPerhydroacenaphthene or dodecahydroacenaphthylene is used in the synthesis of Alkyladamantanes by the passage of the latter over the alumina catalyst in a flow-type plant with a metal reactor that has application in the field of nanotechnology.
PreparationPerhydro acenaphthene is the main raw material of preparation 1,3-dimethyladamantane, is the important intermediate of preparation Derivatives of Adamantane.Derivatives of Adamantane is a kind of excellent antidementia agent, clinical research confirmation its have good efficacy to vascular dementia.
The synthesis of Perhydroacenaphthene:
1) adding industrial acenaphthylene to 95% ethanol, heating, refluxing and dissolving, then cooling, crystallizing, centrifuging to obtain refined acenaphthene, and carrying out distillation recycling of the filtrate;
2) adding the refined acenaphthene and a catalyst Raney Ni into a high-pressure kettle, replacing gas in the kettle with hydrogen, filling hydrogen to make the pressure in the kettle rise to 0.8 MPa, heating up to about 180°C, starting a reaction for 5 h, continuously supplementing hydrogen during the reaction, making the pressure in the kettle rise slowly, and allowing the pressure after the reaction to be 4.0 MPa;
3) cooling after the reaction is finished, filtering the catalyst, and thus obtaining the perhydroacenaphthene.
https://patents.google.com/patent/CN105461499A/en
perhydroacenaphthene Preparation Products And Raw materials
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