(2,4,6-Tri-isopropyl)phenyl)di-cyclohexylphosphine
98%
- Product Code: 68580
Alias:
Dicyclohexyl[2,4,6-tris(1-methylethyl)phenyl]phosphine;
CAS:
303111-96-8
| Molecular Weight: | 400.62 g./mol | Molecular Formula: | C₂₇H₄₅P |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD11656073 | |
| Melting Point: | Boiling Point: | 479.454ºC | |
| Density: | Storage Condition: | Room temperature, inert gas protection |
Product Description:
This chemical is widely used as a ligand in various catalytic processes, particularly in transition metal catalysis. It is highly effective in facilitating cross-coupling reactions, such as Suzuki-Miyaura and Buchwald-Hartwig couplings, due to its sterically demanding and electron-rich properties. Its bulky structure enhances selectivity and efficiency in forming carbon-carbon and carbon-heteroatom bonds, making it valuable in pharmaceutical and fine chemical synthesis. Additionally, it is employed in the development of advanced materials and in academic research to study catalytic mechanisms and optimize reaction conditions.
Product Specification:
| Test | Specification |
|---|---|
| Purity | 97.5 100% |
| Appearance | White to Tan Powder, Crystals, Crystalline Powder and/or Chunks |
| Infrared spectrum | Conforms to Structure |
| Proton NMR spectra | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.500 | 10-20 days | ฿1,820.00 |
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(2,4,6-Tri-isopropyl)phenyl)di-cyclohexylphosphine
This chemical is widely used as a ligand in various catalytic processes, particularly in transition metal catalysis. It is highly effective in facilitating cross-coupling reactions, such as Suzuki-Miyaura and Buchwald-Hartwig couplings, due to its sterically demanding and electron-rich properties. Its bulky structure enhances selectivity and efficiency in forming carbon-carbon and carbon-heteroatom bonds, making it valuable in pharmaceutical and fine chemical synthesis. Additionally, it is employed in the development of advanced materials and in academic research to study catalytic mechanisms and optimize reaction conditions.
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