diazomethane
ethylpropylether
A
Dimethyl ether
B
ethyl methyl ether
C
methyl propyl ether
D
2-butyl ethyl ether
Conditions | Yield |
---|---|
Product distribution; Mechanism; Ambient temperature; Irradiation; | A n/a B 2.4% C 4.4% D 93.2% |
ethylpropylether
diazomethane-d2
A
Dimethyl ether
B
ethyl methyl ether
C
methyl propyl ether
D
2-butyl ethyl ether
Conditions | Yield |
---|---|
Product distribution; Mechanism; Ambient temperature; Irradiation; deuterium distribution; | A n/a B 3.3% C 4.2% D 92.5% |
Conditions | Yield |
---|---|
With hydrogen; palladium dichloride In N,N-dimethyl-formamide under 18751.5 Torr; for 0.666667h; Product distribution; Ambient temperature; various time; | A 2% B 68.4% |
Stage #1: propargyl alcohol methyl ether With pyridine In toluene for 0.166667h; Glovebox; Stage #2: With hydrogen In toluene at 120℃; under 37503.8 Torr; for 12h; Glovebox; |
ethyl methyl ether
diazomethane-d2
A
diethyl ether
B
isopropyl methyl ether
C
ethene
D
Dimethyl ether
E
methyl propyl ether
Conditions | Yield |
---|---|
Product distribution; Mechanism; Ambient temperature; Irradiation; deuterium distribution; | A 29.7% B 17.9% C n/a D 37.2% E 15.2% |
diazomethane
ethyl methyl ether
A
diethyl ether
B
isopropyl methyl ether
C
ethene
D
methyl propyl ether
Conditions | Yield |
---|---|
Product distribution; Mechanism; Ambient temperature; Irradiation; | A 34% B 33.2% C n/a D 32.8% |
A
diethyl ether
B
ethene
C
Dimethyl ether
D
methyl propyl ether
E
trimethylsilyl fluoride
Conditions | Yield |
---|---|
With cesium fluoride Product distribution; Mechanism; | A 1.2% B 3.9% C 2.9% D 0.02% E n/a F n/a |
Conditions | Yield |
---|---|
With naphthalene-2-sulfonate at 122 - 126℃; | |
With benzenesulfonic acid at 122 - 126℃; | |
With naphthalene-2-sulfonate at 122 - 126℃; | |
With benzenesulfonic acid at 122 - 126℃; |
Conditions | Yield |
---|---|
With aluminum oxide; silica gel; zirconium(IV) oxide at 230℃; under 44130.5 Torr; |
methanol
methane
vinyl cation
A
propene
B
1,2-propanediene
C
methyl propyl ether
D
methylallylether
Conditions | Yield |
---|---|
at 100℃; under 60 - 720 Torr; Product distribution; Kinetics; Thermodynamic data; labelled with tritium; -ΔH; |
Conditions | Yield |
---|---|
at 150℃; Yield given; | |
at 150℃; Rate constant; Mechanism; Thermodynamic data; ΔH(excit.), ΔS(excit.); |
methylene
ethylpropylether
A
propene
B
ethene
C
ethyl methyl ether
D
methyl propyl ether
Conditions | Yield |
---|---|
at 20℃; Kinetics; Irradiation; | |
at 100℃; Kinetics; Irradiation; |
Conditions | Yield |
---|---|
In cyclohexane at 20℃; Equilibrium constant; |
Methylethyl-n-propyloxonium Tetrafluoroborate
A
diethyl ether
B
Dimethyl ether
C
ethyl methyl ether
D
methyl propyl ether
Conditions | Yield |
---|---|
With potassium hydroxide In various solvent(s) for 0.5h; Product distribution; Ambient temperature; |
triethylaluminum
chloromethyl methyl ether
A
ethane
B
methyl propyl ether
Conditions | Yield |
---|---|
In 1,2-dimethoxyethane at 60℃; for 2h; |
diethylaluminium chloride
chloromethyl methyl ether
A
ethane
B
methyl propyl ether
Conditions | Yield |
---|---|
In 1,2-dimethoxyethane at 80℃; for 2h; |
chloromethyl methyl ether
sodium tetraethylaluminate
A
ethane
B
methyl propyl ether
Conditions | Yield |
---|---|
In tetrahydrofuran at 60℃; for 5h; |
trimethyl (3-methoxypropyl)tin
A
tetrahydrofuran
B
methyl propyl ether
C
cyclopropyl methyl ether
Conditions | Yield |
---|---|
With benzophenone In benzene at 22℃; for 72h; Irradiation; further reagents (PhCOMe, (t-BuO)2, FeCl3); Yield given. Yields of byproduct given; |
Conditions | Yield |
---|---|
With sodium hydroxide; tetra-(n-butyl)ammonium iodide In chlorobenzene 1.) ice bath, 1h, 2.) water bath, 2h; |
Conditions | Yield |
---|---|
With sodium hydride 1.) 4 h, reflux, 2.) 0.5 h at 20 deg C, reflux, 1 h; Multistep reaction; | |
Stage #1: propan-1-ol With sodium hydride In dimethyl sulfoxide Stage #2: methyl iodide In dimethyl sulfoxide at 20℃; for 5h; Further stages.; |
Conditions | Yield |
---|---|
at 40 - 70℃; Rate constant; Thermodynamic data; Ea, ΔF(excit.), ΔH(excit.), -ΔS(excit.); |
epoxybutene
A
ethyloxirane
B
trans-Crotonaldehyde
C
methyl propyl ether
D
methylallylether
E
butyraldehyde
F
n-butane
Conditions | Yield |
---|---|
With hydrogen; silica gel; palladium at -0.15℃; under 150.012 Torr; Product distribution; Mechanism; also ethyloxirane; also with duterium; also over Pt-SiO2; var. temp. and time; |
methanol
propan-1-ol
A
Dimethyl ether
B
methyl propyl ether
C
Dipropyl ether
Conditions | Yield |
---|---|
at 180 - 185℃; analog reagiert mit Alkohol; |
Conditions | Yield |
---|---|
With aluminum oxide at 180 - 185℃; |
Conditions | Yield |
---|---|
With 1,3,5-triphenylverdazyl at 25℃; Kinetics; Further Variations:; Reaction partners; Temperatures; |
propan-1-ol
A
ethane
B
propane
C
methyl propyl ether
D
Dipropyl ether
Conditions | Yield |
---|---|
With sulfided Ni-Mo; hydrogen at 180℃; under 51714.8 Torr; Product distribution; Further Variations:; Temperatures; |
Dipropyl ether
A
propan-1-ol
B
propane
C
Dimethyl ether
D
methyl propyl ether
Conditions | Yield |
---|---|
With sulfided Ni-Mo; hydrogen at 180℃; under 51714.8 Torr; Product distribution; Further Variations:; Temperatures; |
1,2,3,4-tetrahydrocarbazole
methyl propyl ether
A
1-propyl-1,2,3,4-tetrahydrocarbazole
B
1-ethyl-1,2,3,4-tetrahydrocarbazole
Conditions | Yield |
---|---|
With n-butyllithium; potassium tert-butylate In hexane Ambient temperature; | A n/a B 60% C n/a D n/a |
methyl propyl ether
bis(2,6-di-tert-butyl-4-methylphenoxide)methylaluminum
Conditions | Yield |
---|---|
With tert-butyl methyl ether In hexane addn. of methyl propyl ether and t-butyl methyl ether and MAD (hexane, room temp.), pptn., standing (1 h), heating, redissoln., standing (3 h, room temp.); filtration, elem. anal.; | 60% |
methyl propyl ether
diazomethane-d2
A
butyl methyl ether
B
2-butyl methyl ether
C
Dimethyl ether
D
ethylpropylether
E
isobutyl methyl ether
Conditions | Yield |
---|---|
Product distribution; Mechanism; Ambient temperature; Irradiation; deuterium distribution; | A 32.1% B 20.6% C 4.4% D 23% E 19.9% |
diazomethane
methyl propyl ether
A
butyl methyl ether
B
2-butyl methyl ether
C
ethylpropylether
D
isobutyl methyl ether
Conditions | Yield |
---|---|
Product distribution; Mechanism; Ambient temperature; Irradiation; | A 29.8% B 19.6% C 31.4% D 19.2% |
methyl propyl ether
Conditions | Yield |
---|---|
With aluminium trichloride; aluminium |
methyl propyl ether
phenyl(bromodichloromethyl)mercury
1,1-dichloro-2-methoxy-butane
Conditions | Yield |
---|---|
In benzene |
Conditions | Yield |
---|---|
(i) SbF5, SO2, (ii) /BRN= 1730899/; Multistep reaction; |
Conditions | Yield |
---|---|
Irradiation; |
Conditions | Yield |
---|---|
Irradiation; |
Conditions | Yield |
---|---|
In cyclohexane at 20℃; Equilibrium constant; |
Molecule structure of Methyl propyl ether (CAS NO.557-17-5) :
IUPAC Name: 1-methoxypropane
Molecular Weight: 74.1216 g/mol
Molecular Formula: C4H10O
Density: 0.734 g/cm3
Boiling Point: 40.1 °C at 760 mmHg
Index of Refraction: 1.36
Molar Refractivity: 22.32 cm3
Molar Volume: 100.9 cm3
Polarizability: 8.85×10-24 cm3
Surface Tension: 19 dyne/cm
Enthalpy of Vaporization: 26.75 kJ/mol
log P (octanol-water): 1.21
Water Solubility: 3.05E+04 mg/L
Vapor Pressure: 465 mm Hg
Henry's Law Constant: 1.49E-03 atm-m3/mole
Atmospheric OH Rate Constant: 1.13E-11 cm3/molecule-sec
XLogP3: 1.2
H-Bond Acceptor: 1
Rotatable Bond Count: 2
Exact Mass: 74.073165
MonoIsotopic Mass; 74.073165
Topological Polar Surface Area: 9.2
Heavy Atom Count: 5
Complexity: 13.1
Canonical SMILES: CCCOC
InChI: InChI=1S/C4H10O/c1-3-4-5-2/h3-4H2,1-2H3
InChIKey: VNKYTQGIUYNRMY-UHFFFAOYSA-N
EINECS: 209-158-7
Methyl propyl ether (CAS NO.557-17-5) is an ether once used as a general anaesthetic. It is also used as an alternative to diethyl ether because of its greater potency. Its use as an anaesthetic has since been supplanted by modern halogenated ethers which are much less flammable. Methyl propyl ether (CAS NO.557-17-5) also can be used as a solvent and to make other chemicals.
1. | ihl-mus LC50:259 mg/m3/15M | ANESAV Anesthesiology. 11 (1950),455. |
A poison by inhalation. A flammable liquid. When heated to decomposition it emits acrid smoke and irritating vapors.
Risk Statements: 11
R11:Highly flammable.
Safety Statements: 16-33
S16:Keep away from sources of ignition.
S33:Take precautionary measures against static discharges.
RIDADR: 2612
RTECS: KO2280000
HazardClass: 3.1
PackingGroup: II
DOT Classification: 3; Label: Flammable Liquid
Methyl propyl ether (CAS NO.557-17-5) is also called 1-Methoxypropane ; Methyl n-propyl ether ; Metopryl
Neothyl ; alpha-Methoxy propane ; Propane, 1-methoxy- ; Propane, 1-methoxy- (9CI) . Methyl propyl ether (CAS NO.557-17-5) is a colorless volatile liquid with an ether-like odor. It is less dense than water and insoluble in water. Vapors heavier than air. May be narcotic by inhalation in high concentrations. Methyl propyl ether (CAS NO.557-17-5) is highly flammable. Oxidizes readily in air to form unstable peroxides that may explode spontaneously. A mixture of liquid air and diethyl ether exploded spontaneously. Ethers, such as Methyl propyl ether (CAS NO.557-17-5) , can act as bases. They form salts with strong acids and addition complexes with Lewis acids. The complex between diethyl ether and boron trifluoride is an example. Ethers may react violently with strong oxidizing agents. In other reactions, which typically involve the breaking of the carbon-oxygen bond, ethers are relatively inert. Inhalation or contact with material may irritate or burn skin and eyes. Fire may produce irritating, corrosive and/or toxic gases. Vapors may cause dizziness or suffocation. Runoff from fire control may cause pollution. Will be easily ignited by heat, sparks or flames. Vapors may form explosive mixtures with air. Vapors may travel to source of ignition and flash back. They will spread along ground and collect in low or confined areas (sewers, basements, tanks). Vapor explosion hazard indoors, outdoors or in sewers. Runoff to sewer may create fire or explosion hazard. Containers may explode when heated.
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