Identification | More | [Name]
4-METHOXYPHENETHYL ALCOHOL | [CAS]
702-23-8 | [Synonyms]
2-(4-METHOXYPHENYL)ETHANOL 2-(4-METHOXYPHENYL)ETHYL ALCOHOL 4-(2-HYDROXYETHYL)ANISOLE 4-METHOXYPHENETHYL ALCOHOL 4-METHOXYPHENYLETHYL ALCOHOL AKOS 90987 PMEP P-METHOXYPHENETHYL ALCOHOL 2-(p-Methoxyphenyl)ethanol 2-[p-Methoxyphenyl]ethylalcohol 4-methoxy-benzeneethano 4-methoxybenzeneethanol 4-methoxy-Benzeneethanol 4-Methoxy-beta-phenethyl alcohol Benzeneethanol, 4-methoxy- p-Methoxyphenylethyl alcohol 2-(p-Anisyl)ethanol 2-(4-METHOXYPHENETHYL) ALCOHOL 4-METHOXYPHENETHYL ALCOHOL 96% p-Methoxyphenylethanol | [EINECS(EC#)]
211-866-6 | [Molecular Formula]
C9H12O2 | [MDL Number]
MFCD00002900 | [Molecular Weight]
152.19 | [MOL File]
702-23-8.mol |
Chemical Properties | Back Directory | [Appearance]
clear light brown liquid after melting | [Melting point ]
26-28 °C(lit.)
| [Boiling point ]
334-336 °C(lit.)
| [density ]
1.058±0.06 g/cm3 (20 ºC 760 Torr) | [refractive index ]
1.536-1.538
| [Fp ]
>230 °F
| [storage temp. ]
2-8°C | [solubility ]
Soluble in DMSO, Methanol. | [form ]
Liquid After Melting | [pka]
15.00±0.16(Predicted) | [color ]
Clear light brown | [FreezingPoint ]
23.0 to 28.0 ℃ | [BRN ]
2043563 | [LogP]
1.393 (est) | [CAS DataBase Reference]
702-23-8(CAS DataBase Reference) | [EPA Substance Registry System]
4-Methoxybenzeneethanol (702-23-8) |
Safety Data | Back Directory | [Safety Statements ]
S24/25:Avoid contact with skin and eyes . | [WGK Germany ]
3
| [TSCA ]
Yes | [HS Code ]
29062990 |
Hazard Information | Back Directory | [Chemical Properties]
clear light brown liquid after melting | [Uses]
4-Methoxyphenethyl alcohol has a flavor and aroma of fresh citrus juice and may be used for perfumes, foods, and cosmetics.
| [Synthesis Reference(s)]
Journal of the American Chemical Society, 82, p. 3222, 1960 DOI: 10.1021/ja01497a062 Tetrahedron Letters, 33, p. 7465, 1992 DOI: 10.1016/S0040-4039(00)60796-7 | [General Description]
(R)-1-(4-methoxyphenyl)ethanol {(R)-MOPE, 4-Methoxyphenethyl alcohol, 1-(4-methoxyphenyl)ethanol } is formed during the biocatalytic anti-Prelog enantioselective reduction of 4-methoxyacetophenone (MOAP) using immobilized Trigonopsis variabilis AS2. |
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