Vanadium(V) trichloride oxide

95%

Reagent Code: #245519
label
Alias Vanadium trichloride (V); Vanadium trichloride; Vanadium trichloride monoxide; Vanadium trichloride (V); Vanadium trichloride oxide
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CAS Number 7727-18-6

science Other reagents with same CAS 7727-18-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 173.30 g/mol
Formula VOCl₃
badge Registry Numbers
MDL Number MFCD00011459
thermostat Physical Properties
Melting Point -77 °C(lit.)
Boiling Point 126-127 °C(lit.)
inventory_2 Storage & Handling
Density 1.84 g/mL at 25 °C(lit.)
Storage Room temperature, dry, sealed, inert gas

description Product Description

Used as a catalyst in organic synthesis, particularly in oxidation reactions where selective transformation of hydrocarbons is required. It facilitates the conversion of alcohols to carbonyl compounds and is effective in promoting chlorination and oxychlorination processes. Due to its strong Lewis acidity, it also serves in the activation of halogen-containing compounds in industrial chemical manufacturing. Its reactivity makes it suitable for use in specialized reagents for vanadium-based complex formation in research laboratories.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿580.00
inventory 25g
10-20 days ฿9,400.00
inventory 5g
10-20 days ฿1,990.00

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Vanadium(V) trichloride oxide
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Used as a catalyst in organic synthesis, particularly in oxidation reactions where selective transformation of hydrocarbons is required. It facilitates the conversion of alcohols to carbonyl compounds and is effective in promoting chlorination and oxychlorination processes. Due to its strong Lewis acidity, it also serves in the activation of halogen-containing compounds in industrial chemical manufacturing. Its reactivity makes it suitable for use in specialized reagents for vanadium-based complex format

Used as a catalyst in organic synthesis, particularly in oxidation reactions where selective transformation of hydrocarbons is required. It facilitates the conversion of alcohols to carbonyl compounds and is effective in promoting chlorination and oxychlorination processes. Due to its strong Lewis acidity, it also serves in the activation of halogen-containing compounds in industrial chemical manufacturing. Its reactivity makes it suitable for use in specialized reagents for vanadium-based complex formation in research laboratories.

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