2-(4-OCTYLPHENYL)ETHANOL

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Products Intro: Product Name:2-(4-Octylphenyl)ethanol
CAS:162358-05-6
Purity:98% Min. Package:1G;1KG;100KG
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Products Intro: Product Name:2-(4-OCTYLPHENYL)ETHANOL
CAS:162358-05-6
Purity:99% Package:25KG;5KG;1KG
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Products Intro: Product Name:2-(4-Octylphenyl)ethanol
CAS:162358-05-6
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Products Intro: Product Name:2-(4-OCTYLPHENYL)ETHANOL
CAS:162358-05-6
Purity:97%-99.9% Package:1KG;1USD
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Products Intro: Product Name:2-(4-Octylphenyl)ethan-1-ol
CAS:162358-05-6
Purity:0.99 Remarks:1KG,5KG,25KG,200KG

2-(4-OCTYLPHENYL)ETHANOL manufacturers

2-(4-OCTYLPHENYL)ETHANOL Basic information
Product Name:2-(4-OCTYLPHENYL)ETHANOL
Synonyms:2-(4-OCTYLPHENYL)ETHANOL;Benzeneethanol, 4-octyl;4-Octyl-benzeneethanol;Fingolimod Impurity 46;2-(4-octylphenyl)ethan-1-ol;2-(4-0CTYLPHENYL)ETHANOL;4-Octylphenethyl alcohol
CAS:162358-05-6
MF:C16H26O
MW:234.38
EINECS:
Product Categories:Aromatics Compounds;Aromatics
Mol File:Mol File
2-(4-OCTYLPHENYL)ETHANOL Structure
2-(4-OCTYLPHENYL)ETHANOL Chemical Properties
Boiling point 306.3±10.0℃ (760 Torr)
density 0.931±0.06 g/cm3 (20 ºC 760 Torr)
Fp 116.2±4.2℃
storage temp. Sealed in dry,Room Temperature
solubility Chloroform, Ethyl Acetate, Hexane
form Oil
pka14.92±0.10(Predicted)
AppearanceWhite to off-white Solid
CAS DataBase Reference162358-05-6
Safety Information
MSDS Information
2-(4-OCTYLPHENYL)ETHANOL Usage And Synthesis
Chemical PropertiesOil
Uses2-(4-Octylphenyl)ethanol (cas# 162358-05-6) is a compound useful in organic synthesis.
Synthesis
2-(4-Octylphenyl)ethyl acetate

162358-04-5

2-(4-OCTYLPHENYL)ETHANOL

162358-05-6

The general procedure for the synthesis of 4-dodecylphenylethanol from ethyl-[2-(4-octylphenyl)]acetate was as follows: sodium methanol (195 mg, 3.61 mmol) was added to a methanol (MeOH, 10 mL) solution of ethyl 4-octylphenylacetate (500 mg, 1.81 mmol). The reaction mixture was heated to reflux for 6 hours. Upon completion of the reaction, the solvent was evaporated and the residue was partitioned between ethyl acetate (EtOAc) and water. The organic layer was separated and washed with saturated saline (brine). The organic phase was dried with anhydrous sodium sulfate (Na2SO4), filtered and the solvent was evaporated to give 4-octylphenethyl alcohol (390 mg, 92% yield) as a yellow oil. The product was characterized by 1H NMR (400 MHz, CDCl3): δ 0.88 (t, J = 6.8 Hz, 3H), 1.22-1.30 (m, 10H), 1.55-1.63 (m, 2H), 2.57 (t, J = 7.8 Hz, 2H), 2.83 (t, J = 6.6 Hz, 2H), 3.84 (t, J = 6.6 Hz , 2H), 7.11 (s, 4H).

References[1] Journal of Organic Chemistry, 2004, vol. 69, # 11, p. 3950 - 3952
[2] Chemical Communications, 2013, vol. 49, # 21, p. 2136 - 2138
[3] Patent: WO2014/118556, 2014, A2. Location in patent: Page/Page column 50
[4] Journal of Medicinal Chemistry, 2000, vol. 43, # 15, p. 2946 - 2961
[5] Patent: US2014/235895, 2014, A1. Location in patent: Paragraph 0253
2-(4-OCTYLPHENYL)ETHANOL Preparation Products And Raw materials
Raw materials2-(4-Octylphenyl)ethyl acetate-->Methanol-->Sodium Methoxide
Preparation ProductsN-[1,1-Bis[(acetyloxy)methyl]-3-(4-octylphenyl)propyl]acetamide
Tag:2-(4-OCTYLPHENYL)ETHANOL(162358-05-6) Related Product Information
Fingolimod EP Impurity D Fingolimod Palmitate Amide Fingolimod Impurity 4 Benzene, 1-(2-iodoethyl)-4-octyl- Fingolimod-d4 2-DiMethylaMino FingoliMod FTY720-d4 Hydrochloride diethyl 2-acetamido-2-(4-octylphenethyl)malonate Fingolimod Fingolimod 2-Phenethyl Analog 2-NitrodeaMino FingoliMod 2-(Acetylamino)-2-[2-(4-octylphenyl)-2-oxoethyl]-propanedioic acid 1,3-diethyl ester N-(1-hydroxy-2-(hydroxymethyl)-4-(4-octylphenyl)butan-2-yl)acetamide N-[1,1-Bis[(acetyloxy)methyl]-3-(4-octylphenyl)propyl]acetamide DIMETHYL 2-(HYDROXYIMINO)MALONATE Fingolimod 3-Phenethyl Analog Fingolimod Impurity 42 Fingolimod hydrochloride