Product Name

  • Name

    2-Methoxypropane

  • EINECS 209-937-1
  • CAS No. 598-53-8
  • Article Data32
  • CAS DataBase
  • Density 0.731 g/cm3
  • Solubility
  • Melting Point
  • Formula C4H10O
  • Boiling Point 50.6 °C at 760 mmHg
  • Molecular Weight 74.1228
  • Flash Point
  • Transport Information
  • Appearance
  • Safety
  • Risk Codes
  • Molecular Structure Molecular Structure of 598-53-8 (2-Methoxypropane)
  • Hazard Symbols
  • Synonyms 2-Methoxypropane;2-Propylmethyl ether;Isopropyl methyl ether;Isopryl;Methyl iso-propyl ether;Methyl isopropylether;Ether,isopropyl methyl (6CI,7CI,8CI);
  • PSA 9.23000
  • LogP 1.04120

Synthetic route

2,6-di-tert-butyl-4-methylpyridine
38222-83-2

2,6-di-tert-butyl-4-methylpyridine

methyltriphenylbismuthonium tetrafluoroborate
278172-59-1

methyltriphenylbismuthonium tetrafluoroborate

isopropyl alcohol
67-63-0

isopropyl alcohol

A

isopropyl methyl ether
598-53-8

isopropyl methyl ether

B

2,6-di-tert-butyl-4-methylpyridinium tetrafluoroborate
160142-36-9

2,6-di-tert-butyl-4-methylpyridinium tetrafluoroborate

C

triphenylbismuthane
603-33-8

triphenylbismuthane

Conditions
ConditionsYield
In chloroform-d1 alcohol was added to mixt. (Ph3BiMe)(BF4) and 2,6-di-tert-butyl-4-methylpyridine in CDCl3 and allowed to react at 23°C for 4-7 h; detn. by NMR;A 82%
B 100%
C 100%
methanol
67-56-1

methanol

isopropyloxy(diphenyl)-λ6-sulfanenitrile
143885-03-4

isopropyloxy(diphenyl)-λ6-sulfanenitrile

A

isopropyl methyl ether
598-53-8

isopropyl methyl ether

B

S,S-diphenylsulphoximine
22731-83-5

S,S-diphenylsulphoximine

Conditions
ConditionsYield
at 45℃; for 114h;A 99%
B n/a
aluminum isopropoxide
555-31-7

aluminum isopropoxide

methyl iodide
74-88-4

methyl iodide

isopropyl methyl ether
598-53-8

isopropyl methyl ether

Conditions
ConditionsYield
In N,N-dimethyl-formamide for 48h; Heating;66%
ethyl methyl ether
540-67-0

ethyl methyl ether

diazomethane-d2
14621-84-2

diazomethane-d2

A

diethyl ether
60-29-7

diethyl ether

B

isopropyl methyl ether
598-53-8

isopropyl methyl ether

C

ethene
74-85-1

ethene

D

Dimethyl ether
115-10-6

Dimethyl ether

E

methyl propyl ether
557-17-5

methyl propyl ether

Conditions
ConditionsYield
Product distribution; Mechanism; Ambient temperature; Irradiation; deuterium distribution;A 29.7%
B 17.9%
C n/a
D 37.2%
E 15.2%
ethyl methyl ether
540-67-0

ethyl methyl ether

A

diethyl ether
60-29-7

diethyl ether

B

isopropyl methyl ether
598-53-8

isopropyl methyl ether

C

ethene
74-85-1

ethene

D

methyl propyl ether
557-17-5

methyl propyl ether

Conditions
ConditionsYield
Product distribution; Mechanism; Ambient temperature; Irradiation;A 34%
B 33.2%
C n/a
D 32.8%
aluminum isopropoxide
555-31-7

aluminum isopropoxide

isopropyl methyl ether
598-53-8

isopropyl methyl ether

Conditions
ConditionsYield
With isopropyl alcohol
aluminum isopropoxide
555-31-7

aluminum isopropoxide

isopropyl alcohol
67-63-0

isopropyl alcohol

isopropyl methyl ether
598-53-8

isopropyl methyl ether

isopropyl alcohol
67-63-0

isopropyl alcohol

A

isopropyl methyl ether
598-53-8

isopropyl methyl ether

B

ethene
74-85-1

ethene

C

iso-butanol
78-92-2, 15892-23-6

iso-butanol

D

tert-butyl alcohol
75-65-0

tert-butyl alcohol

Conditions
ConditionsYield
bei der Einw. von Sonnenlicht;
isopropyl alcohol
67-63-0

isopropyl alcohol

isopropyl methyl ether
598-53-8

isopropyl methyl ether

Conditions
ConditionsYield
With 1,2-dimethoxyethane; naphthalene; sodium Behandlung der Loesung mit Dimethylsulfat unterhalb 20grad;
sodium isopropylate
683-60-3

sodium isopropylate

methyl iodide
74-88-4

methyl iodide

isopropyl methyl ether
598-53-8

isopropyl methyl ether

isopropyl alcohol
67-63-0

isopropyl alcohol

methyl iodide
74-88-4

methyl iodide

isopropyl methyl ether
598-53-8

isopropyl methyl ether

Conditions
ConditionsYield
With sodium hydride
With sodium hydride 1.) ether, 4 h, reflux, 2.) 0.5 h at 20 deg C, reflux, 1 h; Multistep reaction;
With diethylene glycol dimethyl ether; sodium hydride
Stage #1: isopropyl alcohol With sodium hydride In dimethyl sulfoxide
Stage #2: methyl iodide In dimethyl sulfoxide at 20℃; for 5h; Further stages.;
methanol
67-56-1

methanol

Methyltriisopropoxyphosphonium tetrafluoroborate
93000-48-7

Methyltriisopropoxyphosphonium tetrafluoroborate

isopropyl methyl ether
598-53-8

isopropyl methyl ether

Conditions
ConditionsYield
at 25℃; for 12h;90 % Spectr.
methoxyl radical
2143-68-2

methoxyl radical

propane
74-98-6

propane

isopropyl methyl ether
598-53-8

isopropyl methyl ether

Conditions
ConditionsYield
Thermodynamic data; Mechanism; calculated (BEBO and equibonding method) activation energies for hydrogen atom transfer reaction, anodic methoxylation;
isopropyl alcohol
67-63-0

isopropyl alcohol

dimethyl sulfate
77-78-1

dimethyl sulfate

isopropyl methyl ether
598-53-8

isopropyl methyl ether

Conditions
ConditionsYield
With sodium hydroxide; tetra-(n-butyl)ammonium iodide In chlorobenzene 1.) ice bath, 1h, 2.) water bath, 2h;
Tetramethyl-[1,2,4,5]tetroxan
1073-91-2

Tetramethyl-[1,2,4,5]tetroxan

A

methanol
67-56-1

methanol

B

biphenyl
92-52-4

biphenyl

C

isopropyl methyl ether
598-53-8

isopropyl methyl ether

D

acetic acid methyl ester
79-20-9

acetic acid methyl ester

E

acetone
67-64-1

acetone

F

toluene
108-88-3

toluene

G

methane, ethane, oxygen, CO2

methane, ethane, oxygen, CO2

Conditions
ConditionsYield
In benzene at 135.5 - 165℃; Rate constant; Product distribution; Mechanism; ΔH(excit.), ΔS(excit.); dependence of kexp from ACDP initial conc. at different temperatures;
propene
187737-37-7

propene

BF3+2CH3OH

BF3+2CH3OH

isopropyl methyl ether
598-53-8

isopropyl methyl ether

Conditions
ConditionsYield
beim Zersetzen des bildenden Anlagerungsprodukts mit Natronlage;
1-(4-ethoxycarbonylphenyl)-3-methyltriazene
54283-75-9

1-(4-ethoxycarbonylphenyl)-3-methyltriazene

isopropyl alcohol
67-63-0

isopropyl alcohol

A

isopropyl methyl ether
598-53-8

isopropyl methyl ether

B

p-aminoethylbenzoate
94-09-7

p-aminoethylbenzoate

C

N2

N2

Conditions
ConditionsYield
copper(II) ion at 35℃; Rate constant; Mechanism;
acetic acid methyl ester
79-20-9

acetic acid methyl ester

isopropyl alcohol
67-63-0

isopropyl alcohol

A

propene
187737-37-7

propene

B

isopropyl methyl ether
598-53-8

isopropyl methyl ether

C

di-isopropyl ether
108-20-3

di-isopropyl ether

D

Isopropyl acetate
108-21-4

Isopropyl acetate

Conditions
ConditionsYield
With sodium oxide; aluminum oxide at 280℃; Product distribution; Further Variations:; different persentage compositions of reactans;
propene
187737-37-7

propene

propane
74-98-6

propane

Dimethyl ether
115-10-6

Dimethyl ether

1,2-propanediene
463-49-0

1,2-propanediene

prop-1-yne
74-99-7

prop-1-yne

A

methanol
67-56-1

methanol

B

isopropyl methyl ether
598-53-8

isopropyl methyl ether

C

di-isopropyl ether
108-20-3

di-isopropyl ether

D

isopropyl alcohol
67-63-0

isopropyl alcohol

E

acetone
67-64-1

acetone

Conditions
ConditionsYield
With hydrogen; hydrogenation catalyst from SCI of Louisville, Ky., USA at 209℃; under 16801.7 Torr;
methanol
67-56-1

methanol

1,2-propanediene
463-49-0

1,2-propanediene

2,2-dimethoxy-propane
77-76-9

2,2-dimethoxy-propane

prop-1-yne
74-99-7

prop-1-yne

A

propene
187737-37-7

propene

B

isopropyl methyl ether
598-53-8

isopropyl methyl ether

C

propane
74-98-6

propane

D

methyl propyl ether
557-17-5

methyl propyl ether

E

acetone
67-64-1

acetone

Conditions
ConditionsYield
Zn-Si catalyst prepared from silicagel and zinc acetate, content of zinc amounts to 20percent converting to ZnO Product distribution / selectivity;
2,2-dimethoxy-propane
77-76-9

2,2-dimethoxy-propane

isopropyl methyl ether
598-53-8

isopropyl methyl ether

Conditions
ConditionsYield
With hydrogen In methanol at 210℃; under 37503.8 - 180018 Torr; for 12h;98 %Chromat.
methanol
67-56-1

methanol

propene
187737-37-7

propene

propane
74-98-6

propane

1,2-propanediene
463-49-0

1,2-propanediene

prop-1-yne
74-99-7

prop-1-yne

A

isopropyl methyl ether
598-53-8

isopropyl methyl ether

B

methyl propyl ether
557-17-5

methyl propyl ether

C

acetone
67-64-1

acetone

Conditions
ConditionsYield
Stage #1: methanol at 170℃; under 5250.53 Torr; for 0.25h;
Stage #2: propene; propane; 1,2-propanediene; prop-1-yne; Zn-Si catalyst prepared from silicagel and zinc acetate, content of zinc amounts to 20percent converting to ZnO at 175 - 220℃; under 5250.53 Torr; for 506h; Product distribution / selectivity;
methylene chloride
74-87-3

methylene chloride

isopropyl alcohol
67-63-0

isopropyl alcohol

isopropyl methyl ether
598-53-8

isopropyl methyl ether

Conditions
ConditionsYield
Stage #1: isopropyl alcohol With methane; dinitrogen monoxide
Stage #2: methylene chloride Kinetics; Thermodynamic data; Gas phase;
isopropyl methyl ether
598-53-8

isopropyl methyl ether

(1R,3R,4S,9R)-6-bromo-5,8-dimethoxy-9-methyl-2,3-dihydro-1,4-(epoxymethano)naphthalene-3,4(1H)-diol
1431636-22-4

(1R,3R,4S,9R)-6-bromo-5,8-dimethoxy-9-methyl-2,3-dihydro-1,4-(epoxymethano)naphthalene-3,4(1H)-diol

(3aR,5S,9bR,10R)-8-bromo-6,9-dimethoxy-2,2,10-trimethyl-4,5-dihydro-3aH-5,9b-(epoxymethano)naphtho[1,2-d][1,3]dioxole
1431636-23-5

(3aR,5S,9bR,10R)-8-bromo-6,9-dimethoxy-2,2,10-trimethyl-4,5-dihydro-3aH-5,9b-(epoxymethano)naphtho[1,2-d][1,3]dioxole

Conditions
ConditionsYield
With toluene-4-sulfonic acid In tetrahydrofuran at 0 - 20℃; for 12h;91%
isopropyl methyl ether
598-53-8

isopropyl methyl ether

(2S,3S,4E)-2,5,9-trimethyldeca-4,8-diene-1,3-diol

(2S,3S,4E)-2,5,9-trimethyldeca-4,8-diene-1,3-diol

(4S,5S)-4-[(1E)-2,6-dimethylhepta-1,5-dienyl]-2,2,5-trimethyl-1,3-dioxane

(4S,5S)-4-[(1E)-2,6-dimethylhepta-1,5-dienyl]-2,2,5-trimethyl-1,3-dioxane

Conditions
ConditionsYield
With pyridinium p-toluenesulfonate In acetone at 20℃; for 3h; Inert atmosphere; Combinatorial reaction / High throughput screening (HTS);90%
isopropyl methyl ether
598-53-8

isopropyl methyl ether

(2S,3S,4Z)-2,5,9-trimethyldeca-4,8-diene-1,3-diol

(2S,3S,4Z)-2,5,9-trimethyldeca-4,8-diene-1,3-diol

(4S,5S)-4-[(1Z)-2,6-dimethylhepta-1,5-dienyl]-2,2,5-trimethyl-1,3-dioxane

(4S,5S)-4-[(1Z)-2,6-dimethylhepta-1,5-dienyl]-2,2,5-trimethyl-1,3-dioxane

Conditions
ConditionsYield
With pyridinium p-toluenesulfonate In acetone at 20℃; for 3h; Inert atmosphere; Combinatorial reaction / High throughput screening (HTS);88%
isopropyl methyl ether
598-53-8

isopropyl methyl ether

2-<(R)-3-benzyloxytetradecanamido>-2-deoxy-D-glucopyranose
111789-76-5, 111789-79-8

2-<(R)-3-benzyloxytetradecanamido>-2-deoxy-D-glucopyranose

2-<(R)-3-(benzyloxy)tetradecanamido>-2-deoxy-4,6-O-isopropylidene-D-glucopyranose
135561-40-9, 135583-79-8

2-<(R)-3-(benzyloxy)tetradecanamido>-2-deoxy-4,6-O-isopropylidene-D-glucopyranose

Conditions
ConditionsYield
With 4 A molecular sieve; toluene-4-sulfonic acid In N,N-dimethyl-formamide for 1h; Ambient temperature;60%
1-methoxy-2-methyl-1-trimethylsiloxy-1-propene
31469-15-5

1-methoxy-2-methyl-1-trimethylsiloxy-1-propene

isopropyl methyl ether
598-53-8

isopropyl methyl ether

methyl 2,2,3-trimethylbut-3-enoate
1727-59-9

methyl 2,2,3-trimethylbut-3-enoate

Conditions
ConditionsYield
With gallium(III) bromide In 1,2-dichloro-ethane at 80℃; for 2h;58%
isopropyl methyl ether
598-53-8

isopropyl methyl ether

2-bromoaniline
615-36-1

2-bromoaniline

2-isopropylamino-1-bromobenzene

2-isopropylamino-1-bromobenzene

Conditions
ConditionsYield
With sodium tetrahydroborate; acetic acid In 1,2-dichloro-ethane at 20℃; for 16h; Inert atmosphere;53%
isopropyl methyl ether
598-53-8

isopropyl methyl ether

isopropyl methyl ether hydrotrioxide
53329-35-4

isopropyl methyl ether hydrotrioxide

Conditions
ConditionsYield
With ozone In acetone at -78℃; Oxidation;40%
isopropyl methyl ether
598-53-8

isopropyl methyl ether

2-O-benzoyl-myo-inositol
156556-46-6

2-O-benzoyl-myo-inositol

2-O-benzoyl-1,6:3,4-di-O-isopropylidene-myo-inositol
208714-30-1

2-O-benzoyl-1,6:3,4-di-O-isopropylidene-myo-inositol

Conditions
ConditionsYield
With toluene-4-sulfonic acid In N,N-dimethyl-formamide at 50℃; for 1.5h; Inert atmosphere;35%
1,2,3,4-tetrahydrocarbazole
942-01-8

1,2,3,4-tetrahydrocarbazole

isopropyl methyl ether
598-53-8

isopropyl methyl ether

A

1-propyl-1,2,3,4-tetrahydrocarbazole
1140-49-4

1-propyl-1,2,3,4-tetrahydrocarbazole

B

1-ethyl-1,2,3,4-tetrahydrocarbazole
10257-86-0

1-ethyl-1,2,3,4-tetrahydrocarbazole

C

1-butyl-1,2,3,4-tetrahydrocarbazole

1-butyl-1,2,3,4-tetrahydrocarbazole

D

1-pentyl-1,2,3,4-tetrahydrocarbazole

1-pentyl-1,2,3,4-tetrahydrocarbazole

Conditions
ConditionsYield
With n-butyllithium; potassium tert-butylate In hexane Ambient temperature;A n/a
B 27%
C n/a
D n/a
isopropyl methyl ether
598-53-8

isopropyl methyl ether

2-chlorobenzalaniline
32347-02-7, 5877-49-6

2-chlorobenzalaniline

(2-Methoxy-2-methyl-1-phenyl-propyl)-phenyl-amine
41203-41-2

(2-Methoxy-2-methyl-1-phenyl-propyl)-phenyl-amine

Conditions
ConditionsYield
With sodium
isopropyl methyl ether
598-53-8

isopropyl methyl ether

2-chlorobenzalaniline
32347-02-7, 5877-49-6

2-chlorobenzalaniline

[1-(2-Chloro-phenyl)-2-methoxy-2-methyl-propyl]-phenyl-amine
41203-42-3

[1-(2-Chloro-phenyl)-2-methoxy-2-methyl-propyl]-phenyl-amine

Conditions
ConditionsYield
With sodium
isopropyl methyl ether
598-53-8

isopropyl methyl ether

phenyl(bromodichloromethyl)mercury
3294-58-4

phenyl(bromodichloromethyl)mercury

1,1-dichloro-2-methoxy-2-methyl-propane
918-43-4

1,1-dichloro-2-methoxy-2-methyl-propane

Conditions
ConditionsYield
In benzene
isopropyl methyl ether
598-53-8

isopropyl methyl ether

2-methoxy-propane-2-sulfinic acid
29099-06-7

2-methoxy-propane-2-sulfinic acid

Conditions
ConditionsYield
With sulfur dioxide Irradiation;
isopropyl methyl ether
598-53-8

isopropyl methyl ether

5-phenyl-3,4-dihydro-2H-pyrrole perchlorate
69105-60-8

5-phenyl-3,4-dihydro-2H-pyrrole perchlorate

A

2-(1-Methoxy-1-methyl-ethyl)-2-phenyl-pyrrolidine
92490-42-1

2-(1-Methoxy-1-methyl-ethyl)-2-phenyl-pyrrolidine

B

2-Isopropoxymethyl-2-phenyl-pyrrolidine

2-Isopropoxymethyl-2-phenyl-pyrrolidine

Conditions
ConditionsYield
In acetonitrile Irradiation;
isopropyl methyl ether
598-53-8

isopropyl methyl ether

(2S,5S)-1,6-bis[(tert-butyldiphenylsilyl)oxy]hexane-2,5-diol
146547-11-7

(2S,5S)-1,6-bis[(tert-butyldiphenylsilyl)oxy]hexane-2,5-diol

1,6-di-O-(tert-butyldiphenyl)silyl-2,5-di-O-isopropylidene-3,4-dideoxy-D-threo-hexitol
146547-12-8

1,6-di-O-(tert-butyldiphenyl)silyl-2,5-di-O-isopropylidene-3,4-dideoxy-D-threo-hexitol

Conditions
ConditionsYield
With toluene-4-sulfonic acid In tetrahydrofuran at 0℃; for 2h;4.11 g
isopropyl methyl ether
598-53-8

isopropyl methyl ether

(3aR,4R,5R,6aS)-4-((1E,5Z)-(S)-3-Hydroxy-octa-1,5-dienyl)-5-(tetrahydro-pyran-2-yloxy)-hexahydro-cyclopenta[b]furan-2-one
32233-42-4

(3aR,4R,5R,6aS)-4-((1E,5Z)-(S)-3-Hydroxy-octa-1,5-dienyl)-5-(tetrahydro-pyran-2-yloxy)-hexahydro-cyclopenta[b]furan-2-one

(3aR,4R,5R,6aS)-4-[(1E,5Z)-(S)-3-(1-Methoxy-1-methyl-ethoxy)-octa-1,5-dienyl]-5-(tetrahydro-pyran-2-yloxy)-hexahydro-cyclopenta[b]furan-2-one
75351-52-9

(3aR,4R,5R,6aS)-4-[(1E,5Z)-(S)-3-(1-Methoxy-1-methyl-ethoxy)-octa-1,5-dienyl]-5-(tetrahydro-pyran-2-yloxy)-hexahydro-cyclopenta[b]furan-2-one

Conditions
ConditionsYield
With toluene-4-sulfonic acid In dichloromethane for 0.166667h; Ambient temperature;

Ether, isopropyl methyl Specification

This chemical is called Ether, isopropyl methyl, and its CAS registry number is 598-53-8. With the molecular formula of C4H10O, its molecular weight is 74.12. It's often used as pharmaceutical intermediates.

Other characteristics of the Ether, isopropyl methyl can be summarised as followings: (1)ACD/LogP: 0.80; (2)# of Rule of 5 Violations: 0; (3)ACD/LogD (pH 5.5): 0.8; (4)ACD/LogD (pH 7.4): 0.8; (5)ACD/BCF (pH 5.5): 2.38; (6)ACD/BCF (pH 7.4): 2.38; (7)ACD/KOC (pH 5.5): 64.68; (8)ACD/KOC (pH 7.4): 64.68; (9)#H bond acceptors: 1; (10)#H bond donors: 0; (11)#Freely Rotating Bonds: 1; (12)Polar Surface Area: 9.23 Å2; (13)Index of Refraction: 1.358; (14)Molar Refractivity: 22.28 cm3; (15)Molar Volume: 101.3 cm3; (16)Polarizability: 8.83×10-24cm3; (17)Surface Tension: 17.8 dyne/cm; (18)Density: 0.731 g/cm3; (19)Flash Point: °C; (20)Enthalpy of Vaporization: 26.05 kJ/mol; (21)Boiling Point: 50.6 °C at 760 mmHg; (22)Vapour Pressure: 299 mmHg at 25°C.

Production method of this chemical: The Ether, isopropyl methyl could be obtained by the reactants of iodomethane and propan-2-ol; aluminium salt. This reaction needs the solvent of dimethylformamide. The yield is 66 %. In addition, this reaction should be taken for 2 days. The other condition is heating.

Uses of this chemical: The Ether, isopropyl methyl could react with 2-[(R)-3-(benzyloxy)tetradecanamido]-2-deoxy-D-glucose, and obtain the 2-[(R)-3-(benzyloxy)tetradecanamido]-2-deoxy-4,6-O-isopropylidene-D-glucopyranose. This reaction needs the reagent of p-toluenesulfonic acid, molecular sieves 4A, and the solvent of dimethylformamide. The yield is 60 %. In addition, this reaction should be taken for 1 hour at the ambient temperature.

You can still convert the following datas into molecular structure:
1.SMILES: O(C(C)C)C
2.InChI: InChI=1/C4H10O/c1-4(2)5-3/h4H,1-3H3
3.InChIKey: RMGHERXMTMUMMV-UHFFFAOYAB

The toxicity data is as follows:

Organism Test Type Route Reported Dose (Normalized Dose) Effect Source
mouse LC50 inhalation 407gm/m3/15M (407000mg/m3) BEHAVIORAL: GENERAL ANESTHETIC Anesthesiology. Vol. 11, Pg. 455, 1950.
Link to PubMed

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