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2-(4-BENZYLOXYPHENYL)ETHANOL

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Products Intro: Product Name:2-(4-(BENZYLOXY)PHENYL)ETHANOL
CAS:61439-59-6
Purity:99% Package:25KG;3USD|5KG;6USD|1KG;9USD
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Products Intro: Product Name:2-(4-Benzyloxyphenyl)ethanol
CAS:61439-59-6
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CAS:61439-59-6
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Products Intro: Product Name:2-(4-Benzyloxyphenyl) Ethanol
CAS:61439-59-6
Purity:0.98 Package:1KG;5KG;25KG

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2-(4-BENZYLOXYPHENYL)ETHANOL Basic information
Product Name:2-(4-BENZYLOXYPHENYL)ETHANOL
Synonyms:4-BENZYLOXYPHENYLETHAN-2-OL;4-BENZYLOXYPHENYLETHYL ALCOHOL;P-Benzyloxyphenylethan-2-ol;2-(4-BENZYLOXYPHENYL)ETHANOL;p-(benzyloxy)phenethyl alcohol;4-Benzyloxyphenethyl Alcohol;2-(4-Benzyloxyphenyl)ethanol, 98+%;-(p-Benzyloxyphenyl)ethyl Alcohol
CAS:61439-59-6
MF:C15H16O2
MW:228.29
EINECS:262-795-2
Product Categories:Benzhydrols, Benzyl & Special Alcohols;Aromatics
Mol File:61439-59-6.mol
2-(4-BENZYLOXYPHENYL)ETHANOL Structure
2-(4-BENZYLOXYPHENYL)ETHANOL Chemical Properties
Melting point 85-87°C
Boiling point 379.1±22.0 °C(Predicted)
density 1.116±0.06 g/cm3(Predicted)
storage temp. Sealed in dry,Room Temperature
solubility Chloroform (Slightly), Methanol (Slightly)
pka14.93±0.10(Predicted)
form Solid
color White to Off-White
BRN 2054624
InChIInChI=1S/C15H16O2/c16-11-10-13-6-8-15(9-7-13)17-12-14-4-2-1-3-5-14/h1-9,16H,10-12H2
InChIKeyJCUJAHLWCDISCC-UHFFFAOYSA-N
SMILESC1(CCO)=CC=C(OCC2=CC=CC=C2)C=C1
CAS DataBase Reference61439-59-6
Safety Information
Safety Statements 24/25
MSDS Information
ProviderLanguage
ALFA English
2-(4-BENZYLOXYPHENYL)ETHANOL Usage And Synthesis
Chemical PropertiesWhite Solid
UsesBetaxolol Impurity
Synthesis
4-BENZYLOXYPHENYLACETIC ACID METHYL ESTER

68641-16-7

2-(4-BENZYLOXYPHENYL)ETHANOL

61439-59-6

Example 2 Synthesis of 2-(4-benzyloxyphenyl)ethanol Methyl 2-(4-benzyloxyphenyl)acetate (7.8 mmol) was dissolved in anhydrous ether (5 mL) and added slowly and dropwise to a suspension of lithium aluminum hydride (15.8 mmol) in anhydrous ether (25 mL) at 0 °C. The reaction mixture was stirred overnight at room temperature and the reaction was subsequently quenched with water. The reaction mixture was extracted with ethyl acetate and the organic layers were combined and dried over anhydrous sodium sulfate. The solvent was removed by distillation under reduced pressure to give 2-(4-phenylmethoxyphenyl)ethanol in quantitative yield. 1H-NMR (CDCl3): δ 7.28-7.47 (m, 5H); 7.17 (d, J = 8.7 Hz, 2H); 6.95 (d, J = 8.7 Hz, 2H); 5.07 (s, 2H); 3.85 (t, J = 6.6 Hz, 2H); 2.84 (t, J = 6.6 Hz, 2H).

References[1] Patent: WO2007/139923, 2007, A1. Location in patent: Page/Page column 77
[2] Monatshefte fur Chemie, 1997, vol. 128, # 8-9, p. 863 - 879
[3] Molecular Crystals and Liquid Crystals (1969-1991), 1991, vol. 206, p. 103 - 116
[4] Bioorganic and Medicinal Chemistry Letters, 2002, vol. 12, # 4, p. 525 - 528
[5] Patent: US4672071, 1987, A
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