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| | 4-METHOXYPHENETHYL ALCOHOL Basic information |
| | 4-METHOXYPHENETHYL ALCOHOL Chemical Properties |
| 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. | Sealed in dry,Room Temperature | | solubility | Soluble in DMSO, Methanol. | | pka | 15.00±0.16(Predicted) | | form | Liquid After Melting | | 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 Statements | 24/25 | | WGK Germany | 3 | | TSCA | TSCA listed | | HS Code | 29062990 |
| | 4-METHOXYPHENETHYL ALCOHOL Usage And Synthesis |
| 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. | | Uses | 2-(4-Methoxyphenyl)ethanol is used as an internal standard in the fluorous biphasic catalysis reaction. It is used in the preparation of 4-(2-iodoethyl)phenol, by refluxing it with 47% hydriodic acid. It may be used in the preparation of (2R*,4R*)-1-n-butyl-2-methyl-4-(2-oxopyrrolidin-1-yl)-6-methoxy-1,2,3,4-tetrahydroquinoline and (2R*,4S*)-1-n-butyl-2-methyl-4-(2-oxopyrrolidin-1-yl)-6-methoxy-1,2,3,4- tetrahydroquinoline. It is used for foods, perfumes, and cosmetics. | | Uses | 4-Methoxyphenethyl alcohol was used in the preparation of 4-(2-iodoethyl)phenol, by refluxing it with 47% hydriodic acid. It may be used in the preparation of (2R*,4R*)-1-n-butyl-2-methyl-4-(2-oxopyrrolidin-1-yl)-6-methoxy-1,2,3,4-tetrahydroquinoline and (2R*,4S*)-1-n-butyl-2-methyl-4-(2-oxopyrrolidin-1-yl)-6-methoxy-1,2,3,4- tetrahydroquinoline. | | 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. |
| | 4-METHOXYPHENETHYL ALCOHOL Preparation Products And Raw materials |
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