Basic information Safety Supplier Related

2-(4-OCTYLPHENYL)ETHANOL

Basic information Safety Supplier Related

2-(4-OCTYLPHENYL)ETHANOL Basic information

Product Name:
2-(4-OCTYLPHENYL)ETHANOL
Synonyms:
  • 2-(4-OCTYLPHENYL)ETHANOL
  • Benzeneethanol, 4-octyl
  • 4-Octyl-benzeneethanol
  • 4-Octylphenethyl alcohol
  • Fingolimod Impurity 46
  • 2-(4-octylphenyl)ethan-1-ol
  • 2-(4-0CTYLPHENYL)ETHANOL
CAS:
162358-05-6
MF:
C16H26O
MW:
234.38
Product Categories:
  • Aromatics Compounds
  • Aromatics
Mol File:
Mol File
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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)
Flash point:
116.2±4.2℃
storage temp. 
Sealed in dry,Room Temperature
solubility 
Chloroform, Ethyl Acetate, Hexane
form 
Oil
pka
14.92±0.10(Predicted)
Appearance
White to off-white Solid
CAS DataBase Reference
162358-05-6
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2-(4-OCTYLPHENYL)ETHANOL Usage And Synthesis

Chemical Properties

Oil

Uses

2-(4-Octylphenyl)ethanol (cas# 162358-05-6) is a compound useful in organic synthesis.

Synthesis

162358-04-5

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

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