Product Name

  • Name

    Cyclodecane

  • EINECS 206-032-3
  • CAS No. 293-96-9
  • Article Data26
  • CAS DataBase
  • Density 0.791 g/cm3
  • Solubility Insoluble in water
  • Melting Point 9-10 °C(lit.)
  • Formula C10H20
  • Boiling Point 200.999 °C at 760 mmHg
  • Molecular Weight 140.269
  • Flash Point 58.781 °C
  • Transport Information
  • Appearance colourless liquid
  • Safety 23-24/25
  • Risk Codes R20; R22
  • Molecular Structure Molecular Structure of 293-96-9 (Cyclodecane)
  • Hazard Symbols
  • Synonyms CYCLODECANE;Cyclodecane, 98+%
  • PSA 0.00000
  • LogP 3.90100

Synthetic route

Cyclohexanone diperoxide
183-84-6

Cyclohexanone diperoxide

A

hexahydro-2H-oxepin-2-one
502-44-3

hexahydro-2H-oxepin-2-one

B

oxacyclododecan-2-one
1725-03-7

oxacyclododecan-2-one

C

cyclodecane
293-96-9

cyclodecane

Conditions
ConditionsYield
With toluene-4-sulfonic acid In 2,2,2-trifluoroethanol at 25℃; for 0.666667h; Reagent/catalyst; Solvent; Temperature;A 31.73%
B 42.5%
C n/a
6-hydroxycyclodecan-1-one
15957-40-1

6-hydroxycyclodecan-1-one

A

11-oxa-bicyclo[4.4.1]undecane
281-66-3

11-oxa-bicyclo[4.4.1]undecane

B

cyclodecane
293-96-9

cyclodecane

Conditions
ConditionsYield
With platinum on activated charcoal at 155℃; Hydrogenation;
2-hydroxycyclodecanone
96-00-4

2-hydroxycyclodecanone

cyclodecane
293-96-9

cyclodecane

Conditions
ConditionsYield
With hydrogenchloride; amalgamated zinc; acetic acid
cyclodecyne
3022-41-1

cyclodecyne

cyclodecane
293-96-9

cyclodecane

Conditions
ConditionsYield
With acetic acid; platinum Hydrogenation;
(+/-)-6-methoxycyclodecanone
76976-65-3

(+/-)-6-methoxycyclodecanone

A

11-oxa-bicyclo[4.4.1]undecane
281-66-3

11-oxa-bicyclo[4.4.1]undecane

B

cyclodecane
293-96-9

cyclodecane

Conditions
ConditionsYield
With platinum on activated charcoal at 155℃; Hydrogenation;
Cyclohexanone diperoxide
183-84-6

Cyclohexanone diperoxide

A

oxacyclododecan-2-one
1725-03-7

oxacyclododecan-2-one

B

cyclodecane
293-96-9

cyclodecane

C

cyclohexanone
108-94-1

cyclohexanone

Conditions
ConditionsYield
In benzene at 140℃; Rate constant; Product distribution; Mechanism; other temperatures; ΔH(excit.), ΔS(excit.);
cis,cis,cis-cyclodeca-1,3,5-triene
75993-36-1

cis,cis,cis-cyclodeca-1,3,5-triene

cyclodecane
293-96-9

cyclodecane

Conditions
ConditionsYield
With hydrogen
trans-tricyclo<7.1.0.04,6>deca-2,7-diene

trans-tricyclo<7.1.0.04,6>deca-2,7-diene

A

cyclodecane
293-96-9

cyclodecane

B

bicyclo<7.1.0>decane
286-76-0, 66537-41-5

bicyclo<7.1.0>decane

C

trans-tricyclo<7.1.0.04,6>decane
286-73-7, 89955-58-8, 89955-59-9

trans-tricyclo<7.1.0.04,6>decane

Conditions
ConditionsYield
With hydrogen; nickel In hexane at 60℃; under 60800 Torr; for 1h; Yields of byproduct given. Title compound not separated from byproducts;
With hydrogen; nickel In hexane at 60℃; under 60800 Torr; for 1h; Yield given. Yields of byproduct given;
With hydrogen; nickel In hexane at 60℃; under 60800 Torr; for 1h; Yield given. Yields of byproduct given. Title compound not separated from byproducts;
Cyclodecene
3618-12-0

Cyclodecene

A

cis-1,2-diethylcyclohexane
824-43-1

cis-1,2-diethylcyclohexane

B

cyclodecane
293-96-9

cyclodecane

trans-N,N'-dimethyl-1,2-cyclohexanediamine
824-43-1, 3642-13-5, 13990-95-9

trans-N,N'-dimethyl-1,2-cyclohexanediamine

Conditions
ConditionsYield
With n-Undecane; (i-PrPCP)IrH2 at 196℃; for 0.5h; Catalytic hydrogenation; Isomerization; Title compound not separated from byproducts;
cyclodec-1c-en-6-yne

cyclodec-1c-en-6-yne

cyclodecane
293-96-9

cyclodecane

Conditions
ConditionsYield
With acetic acid; platinum Hydrogenation;
cyclodecadiene

cyclodecadiene

cyclodecane
293-96-9

cyclodecane

Conditions
ConditionsYield
With diethyl ether; platinum Hydrogenation;
diethyl ether
60-29-7

diethyl ether

bromocyclodecane
2749-64-6

bromocyclodecane

iodine
7553-56-2

iodine

magnesium

magnesium

A

cyclodecane
293-96-9

cyclodecane

B

Cyclodecene
3618-12-0

Cyclodecene

C

cyclodecanecarboxylic acid
3203-36-9

cyclodecanecarboxylic acid

D

dicyclodecyl
120620-90-8

dicyclodecyl

Conditions
ConditionsYield
anschliessend Behandeln mit festem Kohlendioxid;
cyclododecane
294-62-2

cyclododecane

A

1-hexene
592-41-6

1-hexene

B

propene
187737-37-7

propene

C

1-dodecene
112-41-4

1-dodecene

D

ethene
74-85-1

ethene

E

nona-1,8-diene
4900-30-5

nona-1,8-diene

F

cyclodecane
293-96-9

cyclodecane

G

further products

further products

Conditions
ConditionsYield
With water at 670 - 770℃; Thermodynamic data; Kinetics; Product distribution; further objects of study: mechanism, activation energy, frequency factor, dependence of ethylene yield distribution from temperature;
cyclodecane
293-96-9

cyclodecane

cyclodecanol
1502-05-2

cyclodecanol

Conditions
ConditionsYield
With ferredoxin reductase; [2Fe–2S] ferredoxin; cytochrome P450 enzyme CYP101B1 In aq. buffer pH=7.4; Kinetics; Catalytic behavior; Reagent/catalyst; Enzymatic reaction;95%
With NADPH; P450 BM3 mutation of F87A/A328I enzyme In dimethyl sulfoxide for 1h; pH=7.5; aq. phosphate buffer; Enzymatic reaction;
Multi-step reaction with 2 steps
1: cytochrome P450 monooxygenase CYP101B1 from Novosphingobium aromaticivorans; ferredoxin reductase; NADH / aq. buffer / 2 h / 20 °C / pH 7.4 / Enzymatic reaction
2: sodium tetrahydroborate
View Scheme
cyclodecane
293-96-9

cyclodecane

chlorocyclodecane
7541-62-0

chlorocyclodecane

Conditions
ConditionsYield
With N-chloro-succinimide; benzophenone In acetonitrile at 27℃; for 24h; Irradiation; regioselective reaction;95%
4,7-dichloroquinoline
86-98-6

4,7-dichloroquinoline

cyclodecane
293-96-9

cyclodecane

4,7-dichloro-2-cyclodecylquinoline

4,7-dichloro-2-cyclodecylquinoline

Conditions
ConditionsYield
With sodium azide; bis-[(trifluoroacetoxy)iodo]benzene In dichloromethane at 20℃; for 4h;87%
cyclodecane
293-96-9

cyclodecane

phenylethynyl diphenylphosphine oxide
7608-18-6

phenylethynyl diphenylphosphine oxide

2-cyclodecyl-1,3-diphenyl-1H-phosphindole 1-oxide

2-cyclodecyl-1,3-diphenyl-1H-phosphindole 1-oxide

Conditions
ConditionsYield
With di-tert-butyl peroxide; copper(I) bromide at 140℃; for 12h; Schlenk technique; Inert atmosphere;80%
cyclodecane
293-96-9

cyclodecane

C19H16F3N2O2S(1+)*BF4(1-)

C19H16F3N2O2S(1+)*BF4(1-)

4-cyclodecyl-2-phenylpyridine

4-cyclodecyl-2-phenylpyridine

Conditions
ConditionsYield
With 9,10-phenanthrenequinone In acetonitrile at 20℃; for 24h; UV-irradiation; Inert atmosphere;80%
cyclodecane
293-96-9

cyclodecane

2-isocyano-4’,5-dimethyl-1,1’-biphenyl

2-isocyano-4’,5-dimethyl-1,1’-biphenyl

6-cyclodecyl-2,8-dimethylphenanthridine
1620195-63-2

6-cyclodecyl-2,8-dimethylphenanthridine

Conditions
ConditionsYield
With copper(I) oxide; di-tert-butyl peroxide at 120℃; for 24h; Sealed tube;75%
cyclodecane
293-96-9

cyclodecane

1-fluorocyclodecane
860003-06-1

1-fluorocyclodecane

Conditions
ConditionsYield
With Selectfluor; acetophenone In acetonitrile at 27℃; for 15h; Inert atmosphere; Irradiation;73%
With copper(l) iodide; N-hydroxyphthalimide; N,N'-bis(benzyliden)ethylendiamine; Selectfluor; potassium iodide; potassium tetrakis(pentafluorophenyl)borate In acetonitrile at 81℃; for 0.5h; Reagent/catalyst; Inert atmosphere;47%
With 1-(chloromethyl)-4-fluoro-1,4-diazabicyclo[2.2.2]octane-1,4-diium tetrafluoroborate; 1,2,4,5-tetracyanobenzene In acetonitrile for 16h; Inert atmosphere; UV-irradiation;64 %Spectr.
With copper(l) iodide; potassium carbonate; Selectfluor; N,N'-(ethane-1,2-diyl)bis(1-(2,6-dichlorophenyl)methanimine) In [D3]acetonitrile at 20℃; for 0.0333333h; Reagent/catalyst; Inert atmosphere;
With triethyl borane; Selectfluor In hexane; acetonitrile at 20℃; for 4h; Inert atmosphere;40 %Spectr.
cyclodecane
293-96-9

cyclodecane

1-[(triisopropylsilyl)ethynyl]-1,2-benziodoxol-3(1H)-one

1-[(triisopropylsilyl)ethynyl]-1,2-benziodoxol-3(1H)-one

(cyclodecylethynyl)triisopropylsilane

(cyclodecylethynyl)triisopropylsilane

Conditions
ConditionsYield
With di-tert-butyl peroxide at 100℃; for 16h; Schlenk technique; Inert atmosphere;67%
cyclodecane
293-96-9

cyclodecane

methyl isoquinoline-3-carboxylate
27104-73-0

methyl isoquinoline-3-carboxylate

C21H27NO2

C21H27NO2

Conditions
ConditionsYield
With tris(2,2'-bipyridyl)ruthenium dichloride; 4,5,6,7-tetrafluoro-1-hydroxybenzo[d][1,2]iodaoxol-3(1H)-one In dichloromethane at 30℃; Minisci Aromatic Substitution; Inert atmosphere; Irradiation; chemoselective reaction;67%
trifluoromethylsulfinyl chloride
20621-29-8

trifluoromethylsulfinyl chloride

cyclodecane
293-96-9

cyclodecane

cyclodecyl(trifluoromethyl)sulfane

cyclodecyl(trifluoromethyl)sulfane

Conditions
ConditionsYield
With dipotassium peroxodisulfate; triphenylphosphine; silver carbonate In acetonitrile at 60℃; for 12h; Inert atmosphere; Sealed tube;58%
With silver (II) carbonate; dipotassium peroxodisulfate; triphenylphosphine In acetonitrile at 60℃; for 12h; Sealed tube; Inert atmosphere;61 %Spectr.
cyclodecane
293-96-9

cyclodecane

1,10-decanedioic acid
111-20-6

1,10-decanedioic acid

Conditions
ConditionsYield
With N-hydroxyphthalimide; bis(acetylacetonato)manganese(II); oxygen; acetic acid at 100℃; under 760.051 Torr; for 14h;55%
With nitric acid
cyclodecane
293-96-9

cyclodecane

silver(I) trifluoromethanethiolate
811-68-7

silver(I) trifluoromethanethiolate

cyclodecyl(trifluoromethyl)sulfane

cyclodecyl(trifluoromethyl)sulfane

Conditions
ConditionsYield
With dipotassium peroxodisulfate In acetonitrile at 60℃; for 12h; Inert atmosphere; Sealed tube;55%
cyclohexenone
930-68-7

cyclohexenone

cyclodecane
293-96-9

cyclodecane

3-cyclododecylcyclohexanone

3-cyclododecylcyclohexanone

Conditions
ConditionsYield
With benzophenone In benzene for 26h; Irradiation;52%
cyclopent-2-enone
930-30-3

cyclopent-2-enone

cyclodecane
293-96-9

cyclodecane

3-cyclododecylcyclopentanone

3-cyclododecylcyclopentanone

Conditions
ConditionsYield
With benzophenone In benzene for 15h; Irradiation;48%
cyclodecane
293-96-9

cyclodecane

cyclodecanone
1502-06-3

cyclodecanone

Conditions
ConditionsYield
With dihydrogen peroxide; vanadium phosphorus oxide In acetonitrile at 70℃; for 20h;28%
With dihydrogen peroxide; iron(III) chloride In pyridine; acetic acid Mechanism;
With cis-VI(6,6'-Cl2bpy)2O2> In tetrachloromethane; acetonitrile at 20℃; for 0.5h; Oxidation;75 % Chromat.
cyclodecane
293-96-9

cyclodecane

perfluorocyclodecane
95896-73-4

perfluorocyclodecane

Conditions
ConditionsYield
With fluorine; sodium fluoride at -40 - 60℃;14%
cyclodecane
293-96-9

cyclodecane

azulene
275-51-4

azulene

Conditions
ConditionsYield
With pyrographite at 420 - 480℃; oder an Palladium/Kohle;
cyclodecane
293-96-9

cyclodecane

phenyl(bromodichloromethyl)mercury
3294-58-4

phenyl(bromodichloromethyl)mercury

(Dichlormethyl)-cyclodecan
52188-71-3

(Dichlormethyl)-cyclodecan

methanol
67-56-1

methanol

cyclodecane
293-96-9

cyclodecane

A

Cyclodecylmethanol
3668-38-0

Cyclodecylmethanol

B

dicyclodecyl
120620-90-8

dicyclodecyl

C

ethylene glycol
107-21-1

ethylene glycol

Conditions
ConditionsYield
With mercury at 64℃; for 17h; Irradiation; Yield given. Yields of byproduct given;
cyclodecane
293-96-9

cyclodecane

A

cis-decalin
493-01-6

cis-decalin

B

(Z)-cyclodecene
935-31-9

(Z)-cyclodecene

C

trans-cyclodecene
2198-20-1

trans-cyclodecene

D

cis-bicyclo<5.3.0>decane
16189-46-1

cis-bicyclo<5.3.0>decane

Conditions
ConditionsYield
at 25℃; Product distribution; Irradiation; generation of cycloalkyl radicals and carbenes from various cycloalkanes and their termination reactions during radiolysis and photolysis;A 6 % Chromat.
B 28 % Chromat.
C 47 % Chromat.
D 19 % Chromat.
at 25℃; Irradiation; radiolysis; Yield given. Further byproducts given. Yields of byproduct given;
at 25℃; Irradiation; Further byproducts given;A 5 % Chromat.
B 28 % Chromat.
C 47 % Chromat.
D 20 % Chromat.
cyclodecane
293-96-9

cyclodecane

A

(Z)-cyclodecene
935-31-9

(Z)-cyclodecene

B

trans-cyclodecene
2198-20-1

trans-cyclodecene

C

cis-bicyclo<5.3.0>decane
16189-46-1

cis-bicyclo<5.3.0>decane

D

dicyclodecyl
120620-90-8

dicyclodecyl

Conditions
ConditionsYield
at 25℃; Irradiation; radiolysis; Further byproducts given. Yields of byproduct given;
cyclodecane
293-96-9

cyclodecane

dicyclodecyl
120620-90-8

dicyclodecyl

Conditions
ConditionsYield
With mercury at 35℃; for 1h; Rate constant; Irradiation; substrate pressure 1 Torr, dehydrodimerization;
With mercury at 35℃; for 1h; Irradiation;

Cyclodecane Specification

The Cyclodecane, with the CAS registry number 2941-63-1 and EINECS registry number 206-032-3, is a kind of colourless liquid. And it is also incompatible with strong oxidizing agents. The molecular formula of the chemical is C10H20. What's more, while dealing with this chemical, you should avoid contact with skin and eyes, and do not breathe gas/fumes/vapor/spray (appropriate wording to be specified by the manufacturer).

The characteristics of Cyclodecane are as followings: (1)ACD/LogP: 5.27; (2)# of Rule of 5 Violations: 1; (3)ACD/LogD (pH 5.5): 5.271; (4)ACD/LogD (pH 7.4): 5.271; (5)ACD/BCF (pH 5.5): 5968.76; (6)ACD/BCF (pH 7.4): 5968.76; (7)ACD/KOC (pH 5.5): 17553.734; (8)ACD/KOC (pH 7.4): 17553.734; (9)#H bond acceptors: 0; (10)#H bond donors: 0; (11)#Freely Rotating Bonds: 0; (12)Polar Surface Area: 0 Å2; (13)Index of Refraction: 1.433; (14)Molar Refractivity: 46.117 cm3; (15)Molar Volume: 177.407 cm3; (16)Polarizability: 18.282×10-24cm3; (17)Surface Tension: 25.95 dyne/cm; (18)Density: 0.791 g/cm3; (19)Flash Point: 58.781 °C; (20)Enthalpy of Vaporization: 41.934 kJ/mol; (21)Boiling Point: 200.999 °C at 760 mmHg; (22)Vapour Pressure: 0.447 mmHg at 25°C. 

Addtionally, the following datas could be converted into the molecular structure:
(1)SMILES: C1CCCCCCCCC1
(2)InChI: InChI=1/C10H20/c1-2-4-6-8-10-9-7-5-3-1/h1-10H2
(3)InChIKey: LMGZGXSXHCMSAA-UHFFFAOYAE

Post buying leads

About|Contact|Cas|Product Name|Molecular|Country|Encyclopedia

Message|New Cas|MSDS|Service|Advertisement|CAS DataBase|Article Data|Manufacturers | Chemical Catalog

©2008 LookChem.com,License: ICP

NO.:Zhejiang16009103

complaints:service@lookchem.com Desktop View