Chromium(III) chloride tetrahydrofuran complex (1:3)

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Reagent Code: #162503
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CAS Number 10170-68-0

science Other reagents with same CAS 10170-68-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 374.67 g/mol
Formula C₁₂H₂₄Cl₃CrO₃
badge Registry Numbers
MDL Number MFCD00013222
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a catalyst in organic synthesis, particularly in carbon-carbon bond formation reactions. It facilitates coupling reactions such as the Nozaki-Hiyama-Kishi reaction, where it enhances the selective reduction of organic halides in the presence of aldehydes or ketones. Its solubility in organic solvents like tetrahydrofuran makes it suitable for homogeneous catalytic systems. Also employed in the polymerization of certain olefins and in electrochemical processes due to its redox stability. Commonly handled under inert atmosphere because of sensitivity to moisture and air.

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Test Parameter Specification
Appearance Purple to purplish red Solid
Purity (%) 96.5-100%
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,080.00
inventory 5g
10-20 days ฿4,430.00
inventory 10g
10-20 days ฿8,790.00
inventory 25g
10-20 days ฿18,400.00

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Chromium(III) chloride tetrahydrofuran complex (1:3)
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Used as a catalyst in organic synthesis, particularly in carbon-carbon bond formation reactions. It facilitates coupling reactions such as the Nozaki-Hiyama-Kishi reaction, where it enhances the selective reduction of organic halides in the presence of aldehydes or ketones. Its solubility in organic solvents like tetrahydrofuran makes it suitable for homogeneous catalytic systems. Also employed in the polymerization of certain olefins and in electrochemical processes due to its redox stability. Commonly

Used as a catalyst in organic synthesis, particularly in carbon-carbon bond formation reactions. It facilitates coupling reactions such as the Nozaki-Hiyama-Kishi reaction, where it enhances the selective reduction of organic halides in the presence of aldehydes or ketones. Its solubility in organic solvents like tetrahydrofuran makes it suitable for homogeneous catalytic systems. Also employed in the polymerization of certain olefins and in electrochemical processes due to its redox stability. Commonly handled under inert atmosphere because of sensitivity to moisture and air.

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