2-(Diphenylphosphino)-2',4',6'-triisopropylbiphenyl
98%
- Product Code: 68779
CAS:
819867-23-7
| Molecular Weight: | 464.62 g./mol | Molecular Formula: | C₃₃H₃₇P |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2~8℃, dry, sealed |
Product Description:
2-(Diphenylphosphino)-2',4',6'-triisopropylbiphenyl is widely used as a ligand in transition metal catalysis, particularly in cross-coupling reactions. Its bulky structure enhances steric hindrance, improving the efficiency and selectivity of catalytic processes. This compound is especially valuable in palladium-catalyzed reactions, such as Suzuki-Miyaura and Buchwald-Hartwig couplings, where it facilitates the formation of carbon-carbon and carbon-nitrogen bonds. Its stability and electron-donating properties make it a preferred choice for synthesizing complex organic molecules in pharmaceuticals, agrochemicals, and advanced materials. Additionally, it is employed in asymmetric catalysis to produce chiral compounds with high enantiomeric purity.
Product Specification:
| Test | Specification |
|---|---|
| Purity | 97.5 100% |
| Appearance | White solid |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿360.00 |
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| 1.000 | 10-20 days | ฿620.00 |
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| 5.000 | 10-20 days | ฿2,250.00 |
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| 25.000 | 10-20 days | ฿9,300.00 |
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| 100.000 | 10-20 days | ฿28,200.00 |
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2-(Diphenylphosphino)-2',4',6'-triisopropylbiphenyl
2-(Diphenylphosphino)-2',4',6'-triisopropylbiphenyl is widely used as a ligand in transition metal catalysis, particularly in cross-coupling reactions. Its bulky structure enhances steric hindrance, improving the efficiency and selectivity of catalytic processes. This compound is especially valuable in palladium-catalyzed reactions, such as Suzuki-Miyaura and Buchwald-Hartwig couplings, where it facilitates the formation of carbon-carbon and carbon-nitrogen bonds. Its stability and electron-donating properties make it a preferred choice for synthesizing complex organic molecules in pharmaceuticals, agrochemicals, and advanced materials. Additionally, it is employed in asymmetric catalysis to produce chiral compounds with high enantiomeric purity.
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