| Identification | More | [Name]
Allyl phenyl ether | [CAS]
1746-13-0 | [Synonyms]
(2-PROPENYLOXY)BENZENE
ALLYLOXYBENZENE
ALLYL PHENYL ETHER
PHENYL ALLYL ETHER
(2-propenyloxy)-benzen
(prop-2-enyloxy)-benzene
3-Phenoxypropene
Allyl phenoxylate
Ether, allyl phenyl
ether,allylphenyl
Phenyl 2-propenyl ether
Phenylpropenyl ether
USAF do-23
usafdo-23
3-Phenoxy-1-propene
BENZENE,(2-PROPENYLOXY)-
2-propenoxybenzene
Phenylpropenyl ethe
Phenol allyl ether | [EINECS(EC#)]
217-125-3 | [Molecular Formula]
C9H10O | [MDL Number]
MFCD00008644 | [Molecular Weight]
134.18 | [MOL File]
1746-13-0.mol |
| Chemical Properties | Back Directory | [Appearance]
CLEAR COLOURLESS TO VERY SLIGHTLY YELLOW LIQUID | [Melting point ]
90 °C(Solv: water (7732-18-5)) | [Boiling point ]
192 °C(lit.) | [density ]
0.978 g/mL at 25 °C(lit.)
| [refractive index ]
n20/D 1.522(lit.)
| [Fp ]
145 °F
| [storage temp. ]
Keep in dark place,Sealed in dry,Room Temperature | [solubility ]
Insoluble in water, soluble in alcohol and oils | [form ]
clear liquid | [color ]
Colorless to Almost colorless | [Specific Gravity]
0.978 | [Odor]
Ethereal-rosy, green, slightly “gassy”, Geranium-type odor | [Water Solubility ]
insoluble | [Hydrolytic Sensitivity]
1: no significant reaction with aqueous systems | [BRN ]
1905622 | [LogP]
2.940 | [CAS DataBase Reference]
1746-13-0(CAS DataBase Reference) | [NIST Chemistry Reference]
Benzene, (2-propenyloxy)-(1746-13-0) | [EPA Substance Registry System]
1746-13-0(EPA Substance) |
| Safety Data | Back Directory | [Safety Statements ]
S24/25:Avoid contact with skin and eyes . | [RIDADR ]
NA 1993 / PGIII | [WGK Germany ]
3
| [RTECS ]
DA8575000
| [F ]
10-23 | [TSCA ]
Yes | [HS Code ]
29093090 |
| Hazard Information | Back Directory | [Chemical Properties]
CLEAR COLOURLESS TO VERY SLIGHTLY YELLOW LIQUID | [Uses]
Allyl phenyl ether is an pharmaceutical and OLED intermediate. | [Production Methods]
Allyl phenyl ether can be produced from Phenol and Allyl bromide in Acetone, by heating in the presence of Potassium carbonate. | [Synthesis Reference(s)]
Journal of the American Chemical Society, 81, p. 2705, 1959 DOI: 10.1021/ja01520a030
Synthetic Communications, 23, p. 2527, 1993 DOI: 10.1080/00397919308012585
Tetrahedron Letters, 32, p. 6315, 1991 DOI: 10.1016/0040-4039(91)80156-Z |
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