Cyclohexanone diperoxide
A
hexahydro-2H-oxepin-2-one
B
oxacyclododecan-2-one
C
cyclodecane
Conditions | Yield |
---|---|
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
A
11-oxa-bicyclo[4.4.1]undecane
B
cyclodecane
Conditions | Yield |
---|---|
With platinum on activated charcoal at 155℃; Hydrogenation; |
Conditions | Yield |
---|---|
With hydrogenchloride; amalgamated zinc; acetic acid |
Conditions | Yield |
---|---|
With acetic acid; platinum Hydrogenation; |
(+/-)-6-methoxycyclodecanone
A
11-oxa-bicyclo[4.4.1]undecane
B
cyclodecane
Conditions | Yield |
---|---|
With platinum on activated charcoal at 155℃; Hydrogenation; |
Cyclohexanone diperoxide
A
oxacyclododecan-2-one
B
cyclodecane
C
cyclohexanone
Conditions | Yield |
---|---|
In benzene at 140℃; Rate constant; Product distribution; Mechanism; other temperatures; ΔH(excit.), ΔS(excit.); |
cis,cis,cis-cyclodeca-1,3,5-triene
cyclodecane
Conditions | Yield |
---|---|
With hydrogen |
A
cyclodecane
B
bicyclo<7.1.0>decane
C
trans-tricyclo<7.1.0.04,6>decane
Conditions | Yield |
---|---|
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
A
cis-1,2-diethylcyclohexane
B
cyclodecane
trans-N,N'-dimethyl-1,2-cyclohexanediamine
Conditions | Yield |
---|---|
With n-Undecane; (i-PrPCP)IrH2 at 196℃; for 0.5h; Catalytic hydrogenation; Isomerization; Title compound not separated from byproducts; |
cyclodecane
Conditions | Yield |
---|---|
With acetic acid; platinum Hydrogenation; |
cyclodecane
Conditions | Yield |
---|---|
With diethyl ether; platinum Hydrogenation; |
diethyl ether
bromocyclodecane
iodine
A
cyclodecane
B
Cyclodecene
C
cyclodecanecarboxylic acid
D
dicyclodecyl
Conditions | Yield |
---|---|
anschliessend Behandeln mit festem Kohlendioxid; |
cyclododecane
A
1-hexene
B
propene
C
1-dodecene
D
ethene
E
nona-1,8-diene
F
cyclodecane
Conditions | Yield |
---|---|
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; |
Conditions | Yield |
---|---|
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 |
Conditions | Yield |
---|---|
With N-chloro-succinimide; benzophenone In acetonitrile at 27℃; for 24h; Irradiation; regioselective reaction; | 95% |
Conditions | Yield |
---|---|
With sodium azide; bis-[(trifluoroacetoxy)iodo]benzene In dichloromethane at 20℃; for 4h; | 87% |
Conditions | Yield |
---|---|
With di-tert-butyl peroxide; copper(I) bromide at 140℃; for 12h; Schlenk technique; Inert atmosphere; | 80% |
Conditions | Yield |
---|---|
With 9,10-phenanthrenequinone In acetonitrile at 20℃; for 24h; UV-irradiation; Inert atmosphere; | 80% |
cyclodecane
6-cyclodecyl-2,8-dimethylphenanthridine
Conditions | Yield |
---|---|
With copper(I) oxide; di-tert-butyl peroxide at 120℃; for 24h; Sealed tube; | 75% |
cyclodecane
1-fluorocyclodecane
Conditions | Yield |
---|---|
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
Conditions | Yield |
---|---|
With di-tert-butyl peroxide at 100℃; for 16h; Schlenk technique; Inert atmosphere; | 67% |
Conditions | Yield |
---|---|
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% |
Conditions | Yield |
---|---|
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. |
Conditions | Yield |
---|---|
With N-hydroxyphthalimide; bis(acetylacetonato)manganese(II); oxygen; acetic acid at 100℃; under 760.051 Torr; for 14h; | 55% |
With nitric acid |
Conditions | Yield |
---|---|
With dipotassium peroxodisulfate In acetonitrile at 60℃; for 12h; Inert atmosphere; Sealed tube; | 55% |
Conditions | Yield |
---|---|
With benzophenone In benzene for 26h; Irradiation; | 52% |
Conditions | Yield |
---|---|
With benzophenone In benzene for 15h; Irradiation; | 48% |
Conditions | Yield |
---|---|
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
perfluorocyclodecane
Conditions | Yield |
---|---|
With fluorine; sodium fluoride at -40 - 60℃; | 14% |
Conditions | Yield |
---|---|
With pyrographite at 420 - 480℃; oder an Palladium/Kohle; |
cyclodecane
phenyl(bromodichloromethyl)mercury
(Dichlormethyl)-cyclodecan
methanol
cyclodecane
A
Cyclodecylmethanol
B
dicyclodecyl
C
ethylene glycol
Conditions | Yield |
---|---|
With mercury at 64℃; for 17h; Irradiation; Yield given. Yields of byproduct given; |
cyclodecane
A
cis-decalin
B
(Z)-cyclodecene
C
trans-cyclodecene
D
cis-bicyclo<5.3.0>decane
Conditions | Yield |
---|---|
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
A
(Z)-cyclodecene
B
trans-cyclodecene
C
cis-bicyclo<5.3.0>decane
D
dicyclodecyl
Conditions | Yield |
---|---|
at 25℃; Irradiation; radiolysis; Further byproducts given. Yields of byproduct given; |
cyclodecane
dicyclodecyl
Conditions | Yield |
---|---|
With mercury at 35℃; for 1h; Rate constant; Irradiation; substrate pressure 1 Torr, dehydrodimerization; | |
With mercury at 35℃; for 1h; Irradiation; |
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
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