Chromium(III) chloride tetrahydrofuran complex (1:3)
97%
- Product Code: 162503
CAS:
10170-68-0
| Molecular Weight: | 374.67 g./mol | Molecular Formula: | C₁₂H₂₄Cl₃CrO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00013222 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
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.
Product Specification:
| Test | Specification |
|---|---|
| Appearance | Purple to purplish red Solid |
| Purity (%) | 96.5-100% |
| Infrared Spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 1g | 10-20 days | €28.46 |
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| 5g | 10-20 days | €116.74 |
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| 10g | 10-20 days | €231.64 |
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| 25g | 10-20 days | €484.90 |
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Chromium(III) chloride tetrahydrofuran complex (1:3)
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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