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2146-36-3

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  • Perhydroacenaphthene CAS 2146-36-3 Tricyclo[6.3.1.0(4,12)]dodecane IN STOCK Decahydroacenaphthene CAS 2146-36-3

    Cas No: 2146-36-3

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2146-36-3 Usage

Uses

Perhydroacenaphthene 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.

Preparation

Perhydro 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 DEG 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

Check Digit Verification of cas no

The CAS Registry Mumber 2146-36-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,1,4 and 6 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 2146-36:
(6*2)+(5*1)+(4*4)+(3*6)+(2*3)+(1*6)=63
63 % 10 = 3
So 2146-36-3 is a valid CAS Registry Number.
InChI:InChI=1/C12H20/c1-3-9-4-2-6-11-8-7-10(5-1)12(9)11/h9-12H,1-8H2

2146-36-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name perhydroacenaphthene

1.2 Other means of identification

Product number -
Other names Einecs 218-412-6

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:2146-36-3 SDS

2146-36-3Synthetic route

acenaphthene
83-32-9

acenaphthene

decahydroacenaphthene
2146-36-3

decahydroacenaphthene

Conditions
ConditionsYield
100%
aluminum nickel100%
Rh/C100%
1,8-Naphthalic anhydride
81-84-5

1,8-Naphthalic anhydride

decahydroacenaphthene
2146-36-3

decahydroacenaphthene

Conditions
ConditionsYield
With hydrogen; oxygen
(1E,5E,9Z)-cyclododeca-1,5,9-triene
706-31-0

(1E,5E,9Z)-cyclododeca-1,5,9-triene

decahydroacenaphthene
2146-36-3

decahydroacenaphthene

Conditions
ConditionsYield
With hydrogen; nickel 1.) 150 deg C, 4 h, 2.) 200 deg C, 10 h, 150 atm; Yield given. Multistep reaction;
acenaphthene
83-32-9

acenaphthene

A

1-ethylnapthelene
1127-76-0

1-ethylnapthelene

B

decahydroacenaphthene
2146-36-3

decahydroacenaphthene

C

1,2,2a,3,4,5-hexahydro-acenaphthylene
480-72-8

1,2,2a,3,4,5-hexahydro-acenaphthylene

D

2-ethylnaphthalene-1,2,3,4-tetrahydro
32367-54-7, 137823-71-3, 137823-72-4

2-ethylnaphthalene-1,2,3,4-tetrahydro

E

1-ethyltetralin
13556-58-6

1-ethyltetralin

Conditions
ConditionsYield
With aluminum oxide; nickel molybdenum; hydrogen at 390℃; under 45003.6 Torr; for 0.166667h; Product distribution; Kinetics; Mechanism; var. temp., var. time;
acenaphthene
83-32-9

acenaphthene

nickel oxide

nickel oxide

hopcalite/s

hopcalite/s

decahydroacenaphthene
2146-36-3

decahydroacenaphthene

Conditions
ConditionsYield
at 210 - 230℃; under 45600 - 53200 Torr; Hydrogenation;
acenaphthene
83-32-9

acenaphthene

nickel

nickel

decahydroacenaphthene
2146-36-3

decahydroacenaphthene

Conditions
ConditionsYield
at 200℃; under 73550.8 Torr; Hydrogenation;
acenaphthene
83-32-9

acenaphthene

hydrogen

hydrogen

nickel

nickel

A

decahydroacenaphthene
2146-36-3

decahydroacenaphthene

B

1,2,2a,3,4,5-hexahydro-acenaphthylene
480-72-8

1,2,2a,3,4,5-hexahydro-acenaphthylene

Conditions
ConditionsYield
at 150℃;
acenaphthene
83-32-9

acenaphthene

sodium

sodium

hydrogen

hydrogen

A

decahydroacenaphthene
2146-36-3

decahydroacenaphthene

B

1,2,2a,3,4,5-hexahydro-acenaphthylene
480-72-8

1,2,2a,3,4,5-hexahydro-acenaphthylene

Conditions
ConditionsYield
at 300 - 450℃; under 22065.2 Torr;
hydrogenchloride
7647-01-0

hydrogenchloride

acetic acid
64-19-7

acetic acid

acenaphthene quinone
82-86-0

acenaphthene quinone

colloidal platinum

colloidal platinum

A

decahydroacenaphthene
2146-36-3

decahydroacenaphthene

B

2a,3,4,5-tetrahydro-1,2-dihydroxyacenaphthene
16897-64-6

2a,3,4,5-tetrahydro-1,2-dihydroxyacenaphthene

C

tetraoxy compound C24H26O4

tetraoxy compound C24H26O4

Conditions
ConditionsYield
at 60℃; under 2280 Torr; Hydrogenation;
at 60℃; under 2280 Torr; Hydrogenation;
1,2,2a,3,4,5-hexahydro-acenaphthylene
480-72-8

1,2,2a,3,4,5-hexahydro-acenaphthylene

nickel-aluminium oxide

nickel-aluminium oxide

decahydroacenaphthene
2146-36-3

decahydroacenaphthene

Conditions
ConditionsYield
at 140℃; under 22065.2 Torr; Kinetics; Hydrogenation;
acenaphthene
83-32-9

acenaphthene

A

decahydroacenaphthene
2146-36-3

decahydroacenaphthene

B

C12H20
38113-44-9

C12H20

C

C12H20
38113-39-2

C12H20

Conditions
ConditionsYield
With hydrogen In cyclohexane at 200℃; under 60804.1 Torr; for 1h; Temperature;
acenaphthene
83-32-9

acenaphthene

A

decahydroacenaphthene
2146-36-3

decahydroacenaphthene

B

C12H20
38113-44-9

C12H20

C

C12H20
38113-39-2

C12H20

(2aR,8aR)-Dodecahydro-acenaphthylene

(2aR,8aR)-Dodecahydro-acenaphthylene

Conditions
ConditionsYield
With hydrogen In cyclohexane at 150℃; under 60804.1 Torr; for 5h;
acenaphthene
83-32-9

acenaphthene

A

decahydroacenaphthene
2146-36-3

decahydroacenaphthene

B

C12H20
38113-39-2

C12H20

Conditions
ConditionsYield
With hydrogen In cyclohexane at 200℃; under 60804.1 Torr; for 4.5h; Temperature;
decahydroacenaphthene
2146-36-3

decahydroacenaphthene

1,3-dimethyladamantane
702-79-4

1,3-dimethyladamantane

Conditions
ConditionsYield
With aluminium trichloride at 69.85℃; for 50h;90%
With hydrogen fluoride; boron trifluoride Temperature; Autoclave;75%
With Y-zeolite(Na/H 0.97) In hexane at 300℃; for 10h; Concentration; Temperature; Time; Autoclave; Sealed tube;65%
decahydroacenaphthene
2146-36-3

decahydroacenaphthene

A

1,3-dimethyladamantane
702-79-4

1,3-dimethyladamantane

B

1-ethyladamantane
770-69-4

1-ethyladamantane

Conditions
ConditionsYield
With hydrogen fluoride; boron trifluoride at 100℃; for 4h; Temperature; Autoclave;A 77%
B 15%
decahydroacenaphthene
2146-36-3

decahydroacenaphthene

(3,5-dimethyl-1-adamantyl)phosphonous dichloride
82833-87-2

(3,5-dimethyl-1-adamantyl)phosphonous dichloride

Conditions
ConditionsYield
With aluminium trichloride; phosphorus trichloride at 75 - 85℃; for 5h;32%
decahydroacenaphthene
2146-36-3

decahydroacenaphthene

A

toluene
108-88-3

toluene

B

1-indene
95-13-6

1-indene

Conditions
ConditionsYield
at 650℃; beim Cracken;
decahydroacenaphthene
2146-36-3

decahydroacenaphthene

chromium (III)-oxide-aluminium oxide

chromium (III)-oxide-aluminium oxide

acenaphthene
83-32-9

acenaphthene

Conditions
ConditionsYield
at 450℃;
decahydroacenaphthene
2146-36-3

decahydroacenaphthene

1,4-dimethyladamantane
16267-35-9

1,4-dimethyladamantane

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: Y-zeolite(Na/H 0.97) / hexane / 10 h / 300 °C / Autoclave; Sealed tube
2: Y-zeolite(Na/H 0.97) / 2 h / 300 °C
View Scheme
decahydroacenaphthene
2146-36-3

decahydroacenaphthene

A

1,2-dimethyladamantane
16207-81-1

1,2-dimethyladamantane

B

1-ethyladamantane
770-69-4

1-ethyladamantane

C

1,4-dimethyladamantane
16267-35-9

1,4-dimethyladamantane

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: Y-zeolite(Na/H 0.97) / hexane / 10 h / 300 °C / Autoclave; Sealed tube
2: Y-zeolite(Na/H 0.97) / 3 h / 320 °C
View Scheme

2146-36-3Relevant articles and documents

Vapor pressure and liquid heat capacity of perhydroacenaphthylene and perhydrophenanthrene

Rohac, Vladislav,Censky, Miroslav,Zala, Diana,Ruzicka, Vlastimil,Ruzicka, Kvetoslav,Sporka, Karel,Aim, Karel

, p. 1205 - 1210 (2000)

Saturated vapor pressures and liquid heat capacities have been measured for liquid perhydroacenaphthylene and perhydrophenanthrene by comparative ebulliometry over an approximate pressure range from (8 to 100) kPa and by heat conduction calorimetry over a temperature range from about (305 to 335) K. The obtained results for vapor pressures and for heat capacities have been represented within experimental uncertainties by the Antoine and the Cox equations and by an empirical polynomial equation, respectively, and compared with the data available in the literature.

Litvin et al.

, (1979)

A PROCESS FOR PREPARING MEMANTINE

-

Page/Page column 20, (2010/08/08)

The present invention relates to a process for preparing memantine, or a pharmaceutically acceptable salt thereof (e.g., memantine hydrochloride), which is substantially free of impurities.

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