Product Name

  • Name

    Ethyl propenyl ether

  • EINECS 213-176-0
  • CAS No. 928-55-2
  • Article Data21
  • CAS DataBase
  • Density 0.775 g/cm3
  • Solubility soluble in water
  • Melting Point -140°C (estimate)
  • Formula C5H10O
  • Boiling Point 68.2 °C at 760 mmHg
  • Molecular Weight 86.1338
  • Flash Point -2 °F
  • Transport Information UN 3271 3/PG 2
  • Appearance clear colorless to light yellow liquid
  • Safety 16-26-36/37/39-37/39
  • Risk Codes 11-36/37/38
  • Molecular Structure Molecular Structure of 928-55-2 (Ethyl propenyl ether)
  • Hazard Symbols FlammableF,IrritantXi
  • Synonyms Ether,ethyl propenyl (6CI,7CI,8CI);1-Ethoxy-1-propene;1-Ethoxypropene;Ethyl1-propenyl ether;NSC 6107;Ether, ethyl propenyl;
  • PSA 9.23000
  • LogP 1.55650

Synthetic route

3-ethoxyprop-1-ene
557-31-3

3-ethoxyprop-1-ene

ethyl 1-propenyl ether
928-55-2

ethyl 1-propenyl ether

Conditions
ConditionsYield
With diiron nonacarbonyl In benzene at 40 - 50℃; for 2.5h;90%
With triiron dodecarbonyl at 25 - 30℃; for 1h; Irradiation;85%
With potassium tert-butylate In dimethyl sulfoxide at 70℃; for 0.833333h; Inert atmosphere;70%
(PMe3)2Rh(D2O)2*BF4 In water-d2 at 25℃; for 0.5h;95 % Spectr.
1,1-diethoxypropane
4744-08-5

1,1-diethoxypropane

ethyl 1-propenyl ether
928-55-2

ethyl 1-propenyl ether

Conditions
ConditionsYield
2-ethyl-N-(2-ethylhexyl)-1-hexanamine; toluene-4-sulfonic acid77.5%
With quinoline; phosphorus pentoxide distillation at a bath temp. 150 deg C;75%
With quinoline; phosphorus pentoxide vermutlich entsteht als Gemisch von cis- und trans-Form;
With sodium hydrogen sulfate vermutlich entsteht als Gemisch von cis- und trans-Form;
With silver-asbestos at 280℃; vermutlich entsteht als Gemisch von cis- und trans-Form;
3-ethoxy-2-methyl-acrylic acid
23981-30-8

3-ethoxy-2-methyl-acrylic acid

A

ethyl 1-propenyl ether
928-55-2

ethyl 1-propenyl ether

B

methylammonium carbonate
15719-64-9, 15719-76-3, 97762-63-5

methylammonium carbonate

β-ethoxymethacrylic acid

β-ethoxymethacrylic acid

ethyl 1-propenyl ether
928-55-2

ethyl 1-propenyl ether

Conditions
ConditionsYield
bei vorsichtigem Kochen;
propene
187737-37-7

propene

ethyl vinyl ether
109-92-2

ethyl vinyl ether

ethyl 1-propenyl ether
928-55-2

ethyl 1-propenyl ether

Conditions
ConditionsYield
With tricyclohexylphosphine[1,3-bis(2,4,6-trimethylphenyl)-4,5-dihydroimidazol-2-ylidine][benzylidene]ruthenium(II) dichloride In benzene-d6 at 60℃; for 1h;
3-ethoxyprop-1-ene
557-31-3

3-ethoxyprop-1-ene

Triethoxysilane
998-30-1

Triethoxysilane

A

ethylpropylether
628-32-0

ethylpropylether

B

ethyl 1-propenyl ether
928-55-2

ethyl 1-propenyl ether

C

triethoxy(3-ethoxypropyl)silane
81518-55-0

triethoxy(3-ethoxypropyl)silane

Conditions
ConditionsYield
With platinum(0)-1,3-divinyl-1,1,3,3-tetramethyldisiloxane complex In 5,5-dimethyl-1,3-cyclohexadiene; diethylene glycol dimethyl ether at 70℃; for 12h; Inert atmosphere;
...Expand
3-ethoxyprop-1-ene
557-31-3

3-ethoxyprop-1-ene

tris(2-methoxyethoxy)silane
5700-39-0

tris(2-methoxyethoxy)silane

A

ethylpropylether
628-32-0

ethylpropylether

B

ethyl 1-propenyl ether
928-55-2

ethyl 1-propenyl ether

C

C14H32O7Si

C14H32O7Si

Conditions
ConditionsYield
With platinum(0)-1,3-divinyl-1,1,3,3-tetramethyldisiloxane complex In 5,5-dimethyl-1,3-cyclohexadiene; toluene at 70℃; for 12h; Inert atmosphere;
...Expand
ethyl 1-propenyl ether
928-55-2

ethyl 1-propenyl ether

azidoformiate de methyle
1516-56-9

azidoformiate de methyle

[1-Ethoxy-prop-(Z)-ylidene]-carbamic acid methyl ester

[1-Ethoxy-prop-(Z)-ylidene]-carbamic acid methyl ester

Conditions
ConditionsYield
In benzene at 80℃; for 24h;100%
5-iodo-6-methyl-N-[4-(methylsulfonyl)benzyl]-2-oxo-1-[3-(trifluoromethyl)phenyl]-1,2-dihydropyridine-3-carboxamide
694479-85-1

5-iodo-6-methyl-N-[4-(methylsulfonyl)benzyl]-2-oxo-1-[3-(trifluoromethyl)phenyl]-1,2-dihydropyridine-3-carboxamide

ethyl 1-propenyl ether
928-55-2

ethyl 1-propenyl ether

6-methyl-N-[4-(methylsulfonyl)benzyl]-2-oxo-5-propionyl-1-[3-(trifluoromethyl)phenyl]-1,2-dihydropyridine-3-carboxamide

6-methyl-N-[4-(methylsulfonyl)benzyl]-2-oxo-5-propionyl-1-[3-(trifluoromethyl)phenyl]-1,2-dihydropyridine-3-carboxamide

Conditions
ConditionsYield
Stage #1: 5-iodo-6-methyl-N-[4-(methylsulfonyl)benzyl]-2-oxo-1-[3-(trifluoromethyl)phenyl]-1,2-dihydropyridine-3-carboxamide; ethyl 1-propenyl ether With triethylamine; bis[1,2-bis(diphenylphosphino)ethane]palladium(0) In DMF (N,N-dimethyl-formamide) at 100℃;
Stage #2: With hydrogenchloride; water In DMF (N,N-dimethyl-formamide) for 1.5h;		99%
Stage #1: 5-iodo-6-methyl-N-[4-(methylsulfonyl)benzyl]-2-oxo-1-[3-(trifluoromethyl)phenyl]-1,2-dihydropyridine-3-carboxamide; ethyl 1-propenyl ether With triethylamine; bis[1,2-bis(diphenylphosphino)ethane]palladium(0) In DMF (N,N-dimethyl-formamide) at 100℃;
Stage #2: With hydrogenchloride; water In DMF (N,N-dimethyl-formamide) for 1.5h;		99%
ethyl 1-propenyl ether
928-55-2

ethyl 1-propenyl ether

diphenyl ketene
525-06-4

diphenyl ketene

3-ethoxy-4-methyl-2,2-diphenylcyclobutanone
32929-60-5, 32949-69-2, 55701-86-5

3-ethoxy-4-methyl-2,2-diphenylcyclobutanone

Conditions
ConditionsYield
In diethyl ether at 20℃;99%
monomethyl oxalyl chloride
5781-53-3

monomethyl oxalyl chloride

ethyl 1-propenyl ether
928-55-2

ethyl 1-propenyl ether

C8H12O4
1240314-05-9

C8H12O4

Conditions
ConditionsYield
at 0 - 20℃; for 18.33h; Inert atmosphere;97%
ethyl 1-propenyl ether
928-55-2

ethyl 1-propenyl ether

1,3-Dimethyl-6-bromopteridine-2,4(1H,3H)-dione
84689-48-5

1,3-Dimethyl-6-bromopteridine-2,4(1H,3H)-dione

1,3-Dimethyl-6-propionylpteridine-2,4(1H,3H)-dione
71014-17-0

1,3-Dimethyl-6-propionylpteridine-2,4(1H,3H)-dione

Conditions
ConditionsYield
Multistep reaction.;96%
3-methoxy-N,N-dimethylaniline
15799-79-8

3-methoxy-N,N-dimethylaniline

ethyl 1-propenyl ether
928-55-2

ethyl 1-propenyl ether

C21H30N2O2

C21H30N2O2

Conditions
ConditionsYield
With tris(pentafluorophenyl)borate at 110℃; for 8h; Sealed tube;96%
ethyl 1-propenyl ether
928-55-2

ethyl 1-propenyl ether

(1R)-trans-5-methyl-cyclohex-2-enol
116783-31-4

(1R)-trans-5-methyl-cyclohex-2-enol

(3R,5S)-3-(2-Bromo-1-ethoxy-propoxy)-5-methyl-cyclohexene
208761-32-4

(3R,5S)-3-(2-Bromo-1-ethoxy-propoxy)-5-methyl-cyclohexene

Conditions
ConditionsYield
With N-Bromosuccinimide In diethyl ether95%
ethanol
64-17-5

ethanol

ethyl 1-propenyl ether
928-55-2

ethyl 1-propenyl ether

Trichloroacetyl chloride
76-02-8

Trichloroacetyl chloride

(E)-ethyl 3-ethoxy-2-methylacrylate

(E)-ethyl 3-ethoxy-2-methylacrylate

Conditions
ConditionsYield
Stage #1: ethyl 1-propenyl ether; trifluoroacetyl chloride With pyridine at -10 - 20℃; for 20h; Inert atmosphere;
Stage #2: ethanol With sodium ethanolate for 0.5h;		95%
Stage #1: ethyl 1-propenyl ether; trifluoroacetyl chloride With pyridine at -10 - 23℃; for 20h; Inert atmosphere;
Stage #2: ethanol With sodium ethanolate for 0.5h;
...Expand
ethyl 1-propenyl ether
928-55-2

ethyl 1-propenyl ether

sodium ethanolate
141-52-6

sodium ethanolate

Trichloroacetyl chloride
76-02-8

Trichloroacetyl chloride

ethyl (ethoxymethylene)methylacetate
92145-32-9

ethyl (ethoxymethylene)methylacetate

Conditions
ConditionsYield
Stage #1: ethyl 1-propenyl ether; trifluoroacetyl chloride With pyridine at -10 - 23℃; for 20h; Inert atmosphere;
Stage #2: sodium ethanolate In ethanol for 0.5h;		95%
Stage #1: ethyl 1-propenyl ether; trifluoroacetyl chloride With pyridine at -10 - 23℃; for 20h; Inert atmosphere;
Stage #2: sodium ethanolate In ethanol for 0.5h;
Stage #1: ethyl 1-propenyl ether; trifluoroacetyl chloride With pyridine In dichloromethane at -10 - 23℃; for 20h; Inert atmosphere;
Stage #2: sodium ethanolate for 0.5h;
...Expand
ethyl 1-propenyl ether
928-55-2

ethyl 1-propenyl ether

tetraphenyldiphosphine disulfide
1054-60-0

tetraphenyldiphosphine disulfide

(1-ethoxypropane-1,2-diyl)bis(diphenylphosphine sulfide)

(1-ethoxypropane-1,2-diyl)bis(diphenylphosphine sulfide)

Conditions
ConditionsYield
In dichloromethane for 10h; Sealed tube; Inert atmosphere; Irradiation;95%
ethyl 1-propenyl ether
928-55-2

ethyl 1-propenyl ether

(1R,5R)-5-methyl-2-cyclohexenol
73610-84-1

(1R,5R)-5-methyl-2-cyclohexenol

(3R,5R)-3-(2-Bromo-1-ethoxy-propoxy)-5-methyl-cyclohexene
208761-34-6

(3R,5R)-3-(2-Bromo-1-ethoxy-propoxy)-5-methyl-cyclohexene

Conditions
ConditionsYield
With N-Bromosuccinimide In diethyl ether94%
ethyl 1-propenyl ether
928-55-2

ethyl 1-propenyl ether

isobutyryl chloride
79-30-1

isobutyryl chloride

cis-3-ethyloxy-2,2,4-trimethylcyclobutanone
55701-92-3, 90511-10-7, 90511-11-8

cis-3-ethyloxy-2,2,4-trimethylcyclobutanone

Conditions
ConditionsYield
With triethylamine In tetrahydrofuran at 80℃; for 3.5h; Cooling with ice;94%
ethyl 1-propenyl ether
928-55-2

ethyl 1-propenyl ether

Methyl (4α,5α)-4-ethoxy-5-methylcyclopent-1-ene-1-carboxylate
139955-15-0, 140928-61-6

Methyl (4α,5α)-4-ethoxy-5-methylcyclopent-1-ene-1-carboxylate

Conditions
ConditionsYield
diethylaluminium chloride In dichloromethane at -78℃;93%
ethyl 1-propenyl ether
928-55-2

ethyl 1-propenyl ether

(1-tosyl-1H-1,2,3-triazol-4-yl)methyl acetate

(1-tosyl-1H-1,2,3-triazol-4-yl)methyl acetate

trans-6-ethoxy-5-methyl-1-tosyl-1,4,5,6-tetrahydropyridin-3-yl acetate

trans-6-ethoxy-5-methyl-1-tosyl-1,4,5,6-tetrahydropyridin-3-yl acetate

Conditions
ConditionsYield
With dirhodium tetraacetate In toluene at 80℃; for 7h; Diels-Alder Cycloaddition; Inert atmosphere; chemoselective reaction;93%
pentaamminetrifluoromethanesulfonato osmium(III) trifluoromethanesulfonate
83781-30-0

pentaamminetrifluoromethanesulfonato osmium(III) trifluoromethanesulfonate

ethyl 1-propenyl ether
928-55-2

ethyl 1-propenyl ether

[Os(NH3)5(η2-1-ethoxypropene)](OTf)2

[Os(NH3)5(η2-1-ethoxypropene)](OTf)2

Conditions
ConditionsYield
With Zn/Hg In methanol stirring (15 min), filtration; pptn. of filtrate (CH2Cl2,Et2O); elem. anal.;92%
ethyl 1-propenyl ether
928-55-2

ethyl 1-propenyl ether

2,4,7,9-tetramethyl-4,7-dihydroperoxy-5,6-dioxadecane
53151-88-5

2,4,7,9-tetramethyl-4,7-dihydroperoxy-5,6-dioxadecane

2,2-bis(1-ethoxypropylperoxy)-4-methylpentane

2,2-bis(1-ethoxypropylperoxy)-4-methylpentane

Conditions
ConditionsYield
With toluene-4-sulfonic acid In isododecane at 15 - 20℃; for 0.5h;91%
2-chloro-8-methyl-quinoline-3-carbaldehyde
73568-26-0

2-chloro-8-methyl-quinoline-3-carbaldehyde

ethyl 1-propenyl ether
928-55-2

ethyl 1-propenyl ether

3-methyl-1-(4-methylphenyl)-2-pyrazolin-5-one
86-92-0

3-methyl-1-(4-methylphenyl)-2-pyrazolin-5-one

C27H28ClN3O2

C27H28ClN3O2

Conditions
ConditionsYield
With triethylammonium acetate for 0.166667h; Microwave irradiation; Green chemistry;91%
...Expand
ethyl 1-propenyl ether
928-55-2

ethyl 1-propenyl ether

2-(methylsulfanyl)benzaldehyde
7022-45-9

2-(methylsulfanyl)benzaldehyde

2-ethoxy-1-[2-(methylthio)phenyl]butan-1-one

2-ethoxy-1-[2-(methylthio)phenyl]butan-1-one

Conditions
ConditionsYield
With C29H39FO2P2Rh(1+)*C32H12BF24(1-) In acetone at 55℃; for 3h; Inert atmosphere; Glovebox;91%
dimethylketene
598-26-5

dimethylketene

ethyl 1-propenyl ether
928-55-2

ethyl 1-propenyl ether

cis-3-ethyloxy-2,2,4-trimethylcyclobutanone
55701-92-3, 90511-10-7, 90511-11-8

cis-3-ethyloxy-2,2,4-trimethylcyclobutanone

Conditions
ConditionsYield
With triethylamine In various solvent(s)90%
In diethyl ether at 20℃;88%
ethyl 1-propenyl ether
928-55-2

ethyl 1-propenyl ether

2-ethoxycarbonyl-1-cyclopentanone
611-10-9

2-ethoxycarbonyl-1-cyclopentanone

ethyl 1-(1-methyl-2-oxoethyl)-2-oxocyclopentanecarboxylate

ethyl 1-(1-methyl-2-oxoethyl)-2-oxocyclopentanecarboxylate

Conditions
ConditionsYield
With copper diacetate; manganese triacetate In dichloromethane at 40℃;90%
With copper diacetate; manganese triacetate In dichloromethane at 40℃; for 18h;90%
ethyl 1-propenyl ether
928-55-2

ethyl 1-propenyl ether

para-methylphenylmagnesium bromide
4294-57-9

para-methylphenylmagnesium bromide

1-methyl-4-(prop-1-enyl)benzene
2698-14-8

1-methyl-4-(prop-1-enyl)benzene

Conditions
ConditionsYield
With C68H72Cl2N6NiP2 In tetrahydrofuran at 50℃; for 12h; Inert atmosphere;90%
2-chloro-8-methyl-quinoline-3-carbaldehyde
73568-26-0

2-chloro-8-methyl-quinoline-3-carbaldehyde

ethyl 1-propenyl ether
928-55-2

ethyl 1-propenyl ether

edaravone
89-25-8

edaravone

4-(2-chloro-8-methylquinolin-3-yl)-6-ethoxy-3,5-dimethyl-1-phenyl-1,4,5,6-tetrahydropyrano[2,3-c]pyrazole

4-(2-chloro-8-methylquinolin-3-yl)-6-ethoxy-3,5-dimethyl-1-phenyl-1,4,5,6-tetrahydropyrano[2,3-c]pyrazole

Conditions
ConditionsYield
With triethylammonium acetate for 0.183333h; Microwave irradiation; Green chemistry;90%
...Expand
ethyl 1-propenyl ether
928-55-2

ethyl 1-propenyl ether

3-chloro-1H-indole-2-carboxaldehyde
110912-15-7

3-chloro-1H-indole-2-carboxaldehyde

3-methyl-1-(4-methylphenyl)-2-pyrazolin-5-one
86-92-0

3-methyl-1-(4-methylphenyl)-2-pyrazolin-5-one

C25H28ClN3O2

C25H28ClN3O2

Conditions
ConditionsYield
With triethylammonium acetate for 0.15h; Microwave irradiation; Green chemistry;90%
...Expand
diethyl acetal
105-57-7

diethyl acetal

ethyl 1-propenyl ether
928-55-2

ethyl 1-propenyl ether

1,1,3-triethoxy-2-methyl-butane
36551-27-6

1,1,3-triethoxy-2-methyl-butane

Conditions
ConditionsYield
With aluminum (III) chloride at -10 - -5℃; for 0.166667h; Reagent/catalyst; Temperature; Inert atmosphere;88%
With aluminum (III) chloride at -10 - 5℃; for 0.166667h; Reagent/catalyst; Temperature; Inert atmosphere;88%
With iron(III) chloride
With diethyl ether; boron trifluoride at 45 - 50℃;
With boron trifluoride diethyl etherate at 65℃;
ethyl 1-propenyl ether
928-55-2

ethyl 1-propenyl ether

orthoformic acid triethyl ester
122-51-0

orthoformic acid triethyl ester

1,1,3,3-tetraethoxy-2-methyl-propane
10602-37-6

1,1,3,3-tetraethoxy-2-methyl-propane

Conditions
ConditionsYield
Stage #1: ethyl 1-propenyl ether; orthoformic acid triethyl ester With boron trifluoride diethyl etherate at 45℃; for 1h;
Stage #2: With sodium carbonate at 45℃; for 3h;		88%
Stage #1: ethyl 1-propenyl ether; orthoformic acid triethyl ester; boron trifluoride diethyl etherate at 25℃; for 1h;
Stage #2: With sodium carbonate for 1h;		80%
unter Zusatz des Borfluorid-Aether-Addukts;
ethyl 1-propenyl ether
928-55-2

ethyl 1-propenyl ether

S-diethoxycarbonylmethyl O-ethyl dithiocarbonate
218966-77-9

S-diethoxycarbonylmethyl O-ethyl dithiocarbonate

diethyl 2-(1-ethoxypropan-2-yl)malonate
93430-76-3

diethyl 2-(1-ethoxypropan-2-yl)malonate

Conditions
ConditionsYield
With triethyl borane; 4-tert-Butylcatechol In hexane; dichloromethane at 20℃; Giese Free Radical Synthesis; Inert atmosphere;88%
2-chloro-8-methyl-quinoline-3-carbaldehyde
73568-26-0

2-chloro-8-methyl-quinoline-3-carbaldehyde

ethyl 1-propenyl ether
928-55-2

ethyl 1-propenyl ether

1,3-diphenyl-5-oxo-4,5-dihydro-1H-pyrazole
4845-49-2

1,3-diphenyl-5-oxo-4,5-dihydro-1H-pyrazole

C31H28ClN3O2

C31H28ClN3O2

Conditions
ConditionsYield
With triethylammonium acetate for 0.15h; Microwave irradiation; Green chemistry;87%
...Expand
ethyl 1-propenyl ether
928-55-2

ethyl 1-propenyl ether

3-chloro-1H-indole-2-carboxaldehyde
110912-15-7

3-chloro-1H-indole-2-carboxaldehyde

edaravone
89-25-8

edaravone

4-(3-chloro-1H-indol-2-yl)-6-ethoxy-3,5-dimethyl-1-phenyl-1,4,5,6-tetrahydropyrano[2,3-c]pyrazole

4-(3-chloro-1H-indol-2-yl)-6-ethoxy-3,5-dimethyl-1-phenyl-1,4,5,6-tetrahydropyrano[2,3-c]pyrazole

Conditions
ConditionsYield
With triethylammonium acetate for 0.166667h; Microwave irradiation; Green chemistry;87%
...Expand
ethyl 1-propenyl ether
928-55-2

ethyl 1-propenyl ether

2-diazo-1H-phenalene-1,3(2H)-dione
18931-19-6

2-diazo-1H-phenalene-1,3(2H)-dione

9-ethoxy-8-methyl-8,9-dihydro-phenaleno[1,2-b]furan-7-one

9-ethoxy-8-methyl-8,9-dihydro-phenaleno[1,2-b]furan-7-one

Conditions
ConditionsYield
dirhodium tetraacetate Cyclization;86%

Ethyl propenyl ether Chemical Properties

Molecular structure of Ether, ethyl propenyl (CAS NO.928-55-2) is:

Product Name: Ether, ethyl propenyl
CAS Registry Number: 928-55-2
IUPAC Name: (Z)-1-ethoxyprop-1-ene
Molecular Weight: 86.1323 [g/mol]
Molecular Formula: C5H10O
XLogP3-AA: 1.4
H-Bond Donor: 0
H-Bond Acceptor: 1 
EINECS: 213-176-0
Refractive index: n20/D 1.398(lit.)
Storage temp.: Flammables area
Water Solubility: soluble 
Surface Tension: 21 dyne/cm
Density: 0.775 g/cm3
Flash Point: -2 °F
Enthalpy of Vaporization: 29.71 kJ/mol
Boiling Point: 68.2 °C at 760 mmHg
Vapour Pressure: 153 mmHg at 25°C
Classification Code: Skin / Eye Irritant

Ethyl propenyl ether Uses

 Ether, ethyl propenyl (CAS NO.928-55-2) is used in organic synthesis.It is also used in coating, adhesive, additives, plasticizer, etc.

Ethyl propenyl ether Toxicity Data With Reference

Organism Test Type Route Reported Dose (Normalized Dose) Effect Source
rabbit LD50 skin 3970uL/kg (3.97mL/kg)   Toxicology and Applied Pharmacology. Vol. 28, Pg. 313, 1974.
rat LCLo inhalation 8000ppm/4H (8000ppm)   Toxicology and Applied Pharmacology. Vol. 28, Pg. 313, 1974.
rat LD50 oral 4660uL/kg (4.66mL/kg)   Toxicology and Applied Pharmacology. Vol. 28, Pg. 313, 1974.

Ethyl propenyl ether Safety Profile

Hazard Codes: FlammableF, IrritantXi
Risk Statements: 11-36/37/38 
R11:Highly flammable. 
R36/37/38:Irritating to eyes, respiratory system and skin.
Safety Statements: 16-26-36/37/39-37/39 
S16:Keep away from sources of ignition. 
S26: In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. 
S36/37/39:Wear suitable protective clothing, gloves and eye/face protection. 
S37/39:Wear suitable gloves and eye/face protection.
RIDADR: UN 3271 3/PG 2
WGK Germany: 3
RTECS: KO0525000
HazardClass: 3
PackingGroup: II

Ethyl propenyl ether Specification

 Ether, ethyl propenyl , its cas register number is 928-55-2. It also can be called  1-Ethoxy-1-propene ; 1-Ethoxypropene ; Ethyl 1-propenyl ether ; Ethyl propenyl ether ; Propenyl ethyl ether ; 1-Propene, 1-ethoxy- .It is a clear colorless to light yellow liquid.

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