Conditions | Yield |
---|---|
With hydrogen; [Ru2(μ-O2C-C6H4-CO2)2] at 20℃; for 5.4h; Kinetics; Product distribution; Further Variations:; Catalysts; reaction times; | 100% |
With [1,1-(1,3-dimethylimidazol-2-ylidene)(PPh3)-3-(Py)-1,2-RhSB9H8]; hydrogen In dichloromethane-d2 under 3750.38 Torr; for 12h; Catalytic behavior; Time; Inert atmosphere; | 73% |
With hydrogen; palladium | 25% |
triethyl borane
N-Cyclohexylcyclododecylidenamin
A
ethane
B
(Z/E)-(N-Cyclohexyl-1-cyclododecenylamino)diethylboran
Conditions | Yield |
---|---|
With diethylboryl-pivalate at 150℃; for 19h; | A 100% B 96% |
With diethylboryl-pivalate at 110℃; for 24h; Product distribution; reactivity of 1h with pure diethyl(pivaloyloxy)borane, different reaction times; | A 4.78 mmol B n/a |
Conditions | Yield |
---|---|
With oxygen In acetonitrile byproducts: {Co(2,2'-bipyridine)2}(2+); one-electron oxidn. of cis-Co complex by (Fe(phen)3(3+) in presence of O2 at 298 K; monitored by (1)H-NMR; | A <1 B <1 C 100% |
In acetonitrile byproducts: {Co(2,2'-bipyridine)2}(2+); one-electron oxidn. of cis-Co complex by (Fe(phen)3(3+) at 298 K; monitored by (1)H-NMR; | A <1 B <1 C 98% |
Conditions | Yield |
---|---|
With oxygen In acetonitrile byproducts: {Co(2,2'-bipyridine)2}(2+); one-electron oxidn. of cis-Co complex by (Fe(phen)3(3+) in presence of O2 at 298 K; monitored by (1)H-NMR; | A <1 B 100% |
In acetonitrile byproducts: {Co(2,2'-bipyridine)2}(2+); one-electron oxidn. of cis-Co complex by (Fe(phen)3(3+) at 298 K; monitored by (1)H-NMR; | A <1 B 100% |
Conditions | Yield |
---|---|
With perchloric acid; oxygen In acetonitrile Kinetics; in presence of H2O; | A <1 B 100% |
Conditions | Yield |
---|---|
In acetonitrile byproducts: {Co(2,2'-bipyridine)2}(2+); one-electron oxidn. of cis-Co complex by (Fe(bpy)3(3+) at 298 K; monitored by (1)H-NMR; | A <1 B <1 C 100% |
Conditions | Yield |
---|---|
With perchloric acid; oxygen In acetonitrile Kinetics; cleavage of the Co-C bond; slowly; | A 100% B <1 |
With perchloric acid; oxygen In acetonitrile Kinetics; enzyme-catalyzed oxidn. (samll amount of CH4); without HClO4 no catalytic activity; | A 11% B 89% |
In acetonitrile Soln. of complex in MeCN in a sealed Pyrex tube was thermostated at 353 K in an oil bath for 52 h;; An atmospheric pressure of N2 was introduced to the tube; gaseous products were analysed by GLC;; |
Conditions | Yield |
---|---|
In acetonitrile byproducts: {Co(2,2'-bipyridine)2}(2+); one-electron oxidn. of cis-Co complex by (Fe(bpy)3(3+) at 298 K; monitored by (1)H-NMR; | A <1 B 100% |
Conditions | Yield |
---|---|
In tetrachloromethane Irradiation (UV/VIS); Irradiation at 509 nm in CCl4; Estimation of the quantum yield of the photochemical reaction. Yield of the products estimated by g.l.c.; | A 0.02% B <1 C 100% |
Conditions | Yield |
---|---|
With ethenetetracarbonitrile In acetonitrile Kinetics; byproducts: tetracyanoethylene(1-); 298 K; | A n/a B 100% |
With 2,3-dicyano-p-benzoquinone In acetonitrile Kinetics; byproducts: 2,3-dicyano-p-benzoquinone(1-); 298 K; | A n/a B 100% |
With 2,6-dichloro-1,4-benzoquinone; magnesium(II) perchlorate In acetonitrile Kinetics; byproducts: 2,6-dichloro-p-benzoquinone(1-); 298 K; | A n/a B 96% |
Conditions | Yield |
---|---|
react. of the educts in a molar ration of 3:2; | A n/a B 100% |
Conditions | Yield |
---|---|
react. of the educts in a molar ratio of 1:1; | A 100% B n/a |
potassium-2,2-(1,5-cyclooctandiyl)-4,5,5-triethyl-2,5-dihydro-3-methyl-1,2,5-oxoniadiboratolate
A
potassium 2,2-(1,5-cyclooctandiyl)-4,5-diethyl-2,5-dihydro-3-methyl-1,2,5-oxadiboratolate
B
ethane
Conditions | Yield |
---|---|
In neat (no solvent) Ar atmosphere; heating (120-140°C, 1 h); elem. anal.; | A 93% B 100% |
potassium 2,2,3,4,5,5-hexaethyl-2,5-dihydro-1,2,5-oxoniadiboratolate
A
potassium 2,2,3,4,5-pentaethyl-2,5-dihydro-1,2,5-oxadiboratolate
B
ethane
Conditions | Yield |
---|---|
In neat (no solvent) Ar atmosphere; heating (110-115°C, 90 min); elem. anal.; | A 100% B 100% |
Conditions | Yield |
---|---|
With bis(tri-t-butylphosphine)palladium(0); cesium fluoride In tetrahydrofuran; N,N-dimethyl-formamide at 80℃; for 0.0833333h; Inert atmosphere; Schlenk technique; | 100% |
Conditions | Yield |
---|---|
With 1,1,1,2,2,2-hexamethyldisilane; tris(pentafluorophenyl)borate In dichloromethane-d2 at 25℃; for 2h; Concentration; Reagent/catalyst; Solvent; Temperature; Time; | 100% |
Conditions | Yield |
---|---|
With iodine In acetonitrile Kinetics; byproducts: I3(1-), (CH3Co(2,2'-bipyridine)2I)(1+); one-electron oxidn. of cis-Co complex by I2 at 298 K; monitored by (1)H-NMR and UV spect. (361 nm); | A <1 B 0.6% C 99% |
Conditions | Yield |
---|---|
With bromine In acetonitrile one-electron oxidn. of cis-Co complex by Br2 at 298 K; monitored by (1)H-NMR; | A 99% B <1 C 0.24% |
Conditions | Yield |
---|---|
In tetrachloromethane Irradiation (UV/VIS); Irradiation at 509 nm in CCl4; Estimation of the quantum yield of the photochemical reaction. Yield of the products are estimated by g.l.c.; | A <1 B 0.9% C 99% |
Conditions | Yield |
---|---|
With iodine In acetonitrile Kinetics; byproducts: I3(1-); one-electron oxidn. of trans-Co complex by I2 at 298 K; monitored by (1)H-NMR and UV spect. (361 nm); | A 0.34% B 0.06% C 99% |
Conditions | Yield |
---|---|
With bromine In acetonitrile one-electron oxidn. of trans-Co complex by Br2 at 298 K; monitored by (1)H-NMR; | A 99% B 0.15% C <1 |
Conditions | Yield |
---|---|
With hydrogen; Pd/Ag-type catalyst supported on alumina at 30℃; under 750.075 Torr; | 98.2% |
With 5% Pd/C; hydrogen at 49.84℃; for 1h; Catalytic behavior; Gas phase; chemoselective reaction; | 93% |
With hydrogen; palladium/alumina at 80℃; under 300.02 Torr; effect of acetylene pressure on the reaction selectivity and hydrogenation rate; in excess of ethylene; |
Conditions | Yield |
---|---|
With lithium In neat (no solvent) at 140℃; Further byproducts given. Yields of byproduct given; | A n/a B n/a C 98.2% D n/a |
Conditions | Yield |
---|---|
With iodine In benzene at 20℃; for 3h; | A 97% B 98% |
carbon monoxide
A
methane
B
ethane
C
propane
D
carbon dioxide
Conditions | Yield |
---|---|
With hydrogen; nickel at 329.9℃; nickel powder, prepared by evaporation-condensation; Yields of byproduct given; | A 98% B n/a C n/a D n/a E n/a |
Conditions | Yield |
---|---|
In n-heptane at 15 - 50℃; for 3h; Esterification; | A n/a B 98% |
ethyl bromide
trans-NiMe2(triethylphosphine)2
trans-dibromobis(triethylphosphine)nickel(II)
B
methane
C
ethane
D
ethene
Conditions | Yield |
---|---|
In toluene ethyl bromide added into toluene soln. of NiMe2(PEt3)2, stirred at roomtemp. for 24 h; evapd. in vac., crystd. from Et2O-hexane; GLC anal.; | A 66% B 53% C 117 % D 98% |
potassium 2,2,3,5,5-pentaethyl-2,5-dihydro-4-methyl-1,2,5-oxoniadiboratolate
A
potassium 2,2,4,5-tetraethyl-2,5-dihydro-3-methyl-1,2,5-oxadiboratolate
B
potassium 2,2,3,5-tetraethyl-2,5-dihydro-4-methyl-1,2,5-oxadiboratolate
C
ethane
Conditions | Yield |
---|---|
In neat (no solvent) Ar atmosphere; heating (120°C, 5 min); isomer mixt. not sepd.; ratio 3-methyl-/4-methyl-isomer 70/30; elem. anal.; | A n/a B n/a C 98% |
potassium 1,5-cyclooctanediylethylhydroxoborate
A
(1,5-cyclooctanediylboryloxy)sodium
B
ethane
Conditions | Yield |
---|---|
In 1,2,5-trimethyl-benzene Ar atmosphere; heating (100-120°C, 30 min); filtration, repeated washing (pentane), drying (0.001 Torr); elem. anal.; | A 83% B 98% |
triethyl borane
N-Cyclohexylidencyclododecylamin
A
ethane
B
diethylboran
Conditions | Yield |
---|---|
With diethylboryl-pivalate at 100 - 105℃; for 4h; Yield given; | A 97% B n/a |
Conditions | Yield |
---|---|
With 2AlBr3*CBr4; bromine at 55 - 65℃; for 18h; | 100% |
With 2AlBr3*CBr4; bromine at 55 - 65℃; for 18h; Product distribution; Mechanism; different times; | 100% |
Conditions | Yield |
---|---|
With oxygen; V-Mo-Nb-Te oxide | 98% |
at 800℃; under 760.051 Torr; for 1h; Catalytic behavior; Gas phase; Flow reactor; | 84% |
With disulfur; iron(II,III) oxide at 940℃; Reagent/catalyst; Temperature; Flow reactor; | 75.9% |
Reported in EPA TSCA Inventory.
DOT Classification: 2.1; Label: Flammable Gas
This chemical is called Ethane, and its CAS registry number is 74-84-0. With the classification code Simple asphyxiant, its product categories are Refrigerants; Organics; Chemical Synthesis; Compressed and Liquefied Gases; Synthetic Reagents. Additionally, it's colorless gas which is incompatible with strong oxidizing agents. It could be produced by the method of cracked gas and cryogenic. However, this chemical is highly flammable and it will readily form explosive mixtures with air.
Other characteristics of the Ethane can be summarised as followings: (1)ACD/LogP: 1.73; (2)# of Rule of 5 Violations: 0; (3)ACD/LogD (pH 5.5): 1.726; (4)ACD/LogD (pH 7.4): 1.726; (5)ACD/BCF (pH 5.5): 12.075; (6)ACD/BCF (pH 7.4): 12.075; (7)ACD/KOC (pH 5.5): 207.034; (8)ACD/KOC (pH 7.4): 207.034; (9)#H bond acceptors: 0; (10)#H bond donors: 0; (11)#Freely Rotating Bonds: 0 ; (12)Index of Refraction: 1.294; (13)Molar Refractivity: 11.315 cm3; (14)Molar Volume: 61.549 cm3; (15)Polarizability: 4.485×10-24cm3; (16)Surface Tension: 10.857 dyne/cm; (17)Density: 0.489 g/cm3; (18)Flash Point: °C; (19)Enthalpy of Vaporization: 16.84 kJ/mol; (20)Boiling Point: °C at 760 mmHg; (21)Vapour Pressure: 28534.01 mmHg at 25°C.
Production method of this chemical: The Ethane could be obtained by the reactant of ethene. This reaction needs the reagents of Pd and hydrogen.
Uses of this chemical: The ethane is widely used as a standard gas, etching gas, standard gas-line instrumentation, the evaluation of the catalyst gas in the chemical industry, metallurgy, electronics, oil and other industrial sectors and scientific research, aviation, atomic energy and other fields. It's also mainly used as raw material for the production of ethylene and for the manufacture of oxide and ethyl bromide and so on in petrochemical industry. In addition, it could be used for making bromoethane. This reaction needs the reagent of CBr4*2AlBr3 and the temperature of 55-60 °C. The yield is 60 %.
When you are using this chemical, please be cautious about it as the following: This chemical is extremely flammable. Keep it away from sources of ignition. Please take precautionary measures against static discharges and keep the container in a well-ventilated place.
You can still convert the following datas into molecular structure:
1.SMILES: CC
2.InChI: InChI=1/C2H6/c1-2/h1-2H3
3.InChIKey: OTMSDBZUPAUEDD-UHFFFAOYAK
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