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21252-69-7

  • Product Name1-Octyl-1H-imidazole
  • Molecular FormulaC11H20N2
  • Molecular Weight180.293
  • Purity99%
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Product Details

Quick Details

  • CasNo: 21252-69-7
  • Molecular Formula: C11H20N2
  • Purity: 99%

Cost-effective and customizable 1-Octyl-1H-imidazole 21252-69-7 in stock

  • Molecular Formula:C11H20N2
  • Molecular Weight:180.293
  • Vapor Pressure:0.00178mmHg at 25°C 
  • Refractive Index:1.499 
  • Boiling Point:302.4 °C at 760 mmHg 
  • PKA:7.09±0.10(Predicted) 
  • Flash Point:136.7 °C 
  • PSA:17.82000 
  • Density:0.92 g/cm3 
  • LogP:3.24360 

1-OCTYLIMIDAZOLE(Cas 21252-69-7) Usage

General Description

1-Octylimidazole is a widely used chemical compound with the molecular formula C12H21N2. It appears as a light yellow to brown clear liquid with a low melting and boiling point. 1-OCTYLIMIDAZOLE is primarily known for its role in chemical synthesis, particularly as a catalyst. Its solubility properties make it ideal for use in the manufacture of a variety of products ranging from pharmaceuticals to plastics. It is known for being stable under normal temperatures and pressures, however, it may pose certain health risks including skin and eye irritation or damage to organs through prolonged or repeated exposure.

InChI:InChI=1/C11H20N2/c1-2-3-4-5-6-7-9-13-10-8-12-11-13/h8,10-11H,2-7,9H2,1H3

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21252-69-7 Process route

1H-imidazole
288-32-4

1H-imidazole

1-bromo-octane
111-83-1

1-bromo-octane

N-octylimidazole
21252-69-7

N-octylimidazole

Conditions
Conditions Yield
With potassium hydroxide; at 80 ℃; for 6h;
90%
With ethanol; sodium; at 65 ℃; for 20h;
90%
1H-imidazole; With sodium hydroxide; In dimethyl sulfoxide; at 90 ℃; for 2h;
1-bromo-octane; In dimethyl sulfoxide; at 20 - 65 ℃; for 19h;
89%
1H-imidazole; With sodium hydroxide; In dimethyl sulfoxide; at 90 ℃; for 2h;
1-bromo-octane; In dimethyl sulfoxide; at 20 - 65 ℃; for 19h;
89%
With sodium hydroxide; In dimethyl sulfoxide; at 20 - 25 ℃; Inert atmosphere;
87.7%
With sodium hydroxide; In tetrahydrofuran; for 72h; Reflux;
86%
With sodium hydroxide; In tetrahydrofuran; water; Reflux;
85%
With propan-1-ol; sodium; Heating;
83%
1H-imidazole; With potassium hydroxide; In dimethyl sulfoxide; at 20 ℃; for 2h;
1-bromo-octane; In dimethyl sulfoxide; for 4h;
82.3%
1H-imidazole; With sodium hydride; In 1,4-dioxane; at 90 ℃; for 1h;
1-bromo-octane; In 1,4-dioxane; at 90 ℃; for 48h;
80%
1H-imidazole; With potassium carbonate; potassium hydroxide; In dichloromethane; for 0.25h;
1-bromo-octane; With tetra-(n-butyl)ammonium iodide; In dichloromethane;
75%
In toluene; for 4h; Reflux;
70%
With sodium hydroxide; tetraethylammonium iodide; In toluene; Heating;
64%
With potassium carbonate; In acetone; Reflux;
62%
With potassium carbonate; In acetone; for 24h; Reflux;
62%
1H-imidazole; With sodium hydride; In tetrahydrofuran; for 0.75h; Inert atmosphere; Cooling with ice;
1-bromo-octane; In tetrahydrofuran; at 20 ℃; for 24h; Inert atmosphere;
60%
1H-imidazole; With sodium hydrogencarbonate; In water; acetone; at 25 ℃; for 1h; Inert atmosphere;
1-bromo-octane; In water; acetone; at 50 ℃; for 20h; Inert atmosphere;
60%
1H-imidazole; With potassium hydroxide; In methanol; water; at 100 ℃;
1-bromo-octane; In methanol; water; at 100 ℃; for 3h;
50%
In ethyl acetate; Heating;
With sodium hydride; In tetrahydrofuran; for 24h; Heating;
With potassium hydroxide; potassium carbonate; tetrabutylammomium bromide; for 0.0333333h; microwave irradiation;
With potassium carbonate; In acetone; Reflux;
1H-imidazole; 1-bromo-octane; In tetrahydrofuran; at 20 ℃; for 48h;
With sodium hydroxide; In tetrahydrofuran; for 12h;
1H-imidazole; With sodium methylate; In methanol;
1-bromo-octane; In methanol; at 65 ℃; for 6h;
1-bromo-octane; In N,N-dimethyl-formamide;
1H-imidazole; With sodium hydride; In N,N-dimethyl-formamide; at 60 ℃; for 6h;
1H-imidazole; With potassium hydroxide; In dimethyl sulfoxide; at 20 ℃; for 0.5h;
1-bromo-octane; In dimethyl sulfoxide; at 18 ℃;
1H-imidazole; With sodium methylate; for 8h;
1-bromo-octane; In ethanol; for 48h;
With potassium hydroxide; In acetonitrile; for 4h; Reflux;
1H-imidazole; With potassium hydroxide; In dimethyl sulfoxide;
1-bromo-octane; In dimethyl sulfoxide; at 18 ℃; for 2h;
With sodium hydroxide; In acetone; at 20 ℃; for 12h; Reagent/catalyst;
With potassium hydroxide; In N,N-dimethyl-formamide; at 120 ℃; for 16h; Schlenk technique;
1H-imidazole; With sodium hydroxide; In tetrahydrofuran; methanol; at 20 ℃; for 1h;
1-bromo-octane; In tetrahydrofuran; methanol; at 60 ℃; for 16h;
1H-imidazole; With sodium hydroxide; In dimethyl sulfoxide; at 90 ℃; for 2h;
1-bromo-octane; In dimethyl sulfoxide; at 20 - 65 ℃; for 19h;
With tetraethylammonium iodide; sodium hydroxide; In toluene; for 10h; Reflux;
1H-imidazole; With sodium; In ethanol; for 2h; Reflux; Inert atmosphere;
1-bromo-octane; In ethanol; for 2h; Reflux; Inert atmosphere;
With potassium hydroxide; In dimethyl sulfoxide;
1H-imidazole
288-32-4

1H-imidazole

1-Bromoheptane
629-04-9

1-Bromoheptane

N-octylimidazole
21252-69-7

N-octylimidazole

Conditions
Conditions Yield
With potassium carbonate; In acetone; Reflux;
80%

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