(1,10-Phenanthroline)(trifluoromethyl)(triphenylphosphine)copper(I)
≥95%
- Product Code: 78956
CAS:
1334890-93-5
| Molecular Weight: | 5755 g./mol | Molecular Formula: | C₃₁H₂₃CuF₃N₂P |
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| Density: | Storage Condition: | room temperature |
Product Description:
This chemical is primarily used in organic synthesis and catalysis, particularly in reactions involving the formation of carbon-carbon or carbon-heteroatom bonds. Its unique structure, combining a phenanthroline ligand with copper and triphenylphosphine, makes it effective in facilitating cross-coupling reactions, such as the Sonogashira or Heck reactions. It is also employed in the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals, due to its ability to stabilize reactive intermediates and enhance reaction selectivity. Additionally, it finds application in materials science for the development of copper-based catalysts used in polymerization processes or the creation of advanced functional materials. Its trifluoromethyl group further enhances its utility in fluorination reactions, which are critical in the production of fluorinated compounds with applications in medicinal chemistry and materials engineering.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | Light yellow to Brown powder to crystal |
| PURITY | 95-100 |
| Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.200 | 10-20 days | Ft45,035.77 |
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| 1.000 | 10-20 days | Ft139,955.66 |
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(1,10-Phenanthroline)(trifluoromethyl)(triphenylphosphine)copper(I)
This chemical is primarily used in organic synthesis and catalysis, particularly in reactions involving the formation of carbon-carbon or carbon-heteroatom bonds. Its unique structure, combining a phenanthroline ligand with copper and triphenylphosphine, makes it effective in facilitating cross-coupling reactions, such as the Sonogashira or Heck reactions. It is also employed in the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals, due to its ability to stabilize reactive intermediates and enhance reaction selectivity. Additionally, it finds application in materials science for the development of copper-based catalysts used in polymerization processes or the creation of advanced functional materials. Its trifluoromethyl group further enhances its utility in fluorination reactions, which are critical in the production of fluorinated compounds with applications in medicinal chemistry and materials engineering.
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