(3-Bromophenyl)diphenylphosphine Oxide
98%
- Product Code: 68626
CAS:
10212-04-1
| Molecular Weight: | 357.19 g./mol | Molecular Formula: | C₁₈H₁₄BrOP |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | 95°C | Boiling Point: | 507.4±42.0°C(Predicted) |
| Density: | 1.43±0.1g/cm3(Predicted) | Storage Condition: | room temperature, dry |
Product Description:
Widely used as a ligand in transition metal catalysis, particularly in cross-coupling reactions such as Suzuki-Miyaura and Heck reactions, where it enhances the efficiency and selectivity of the process. It is also employed in organic synthesis for the preparation of complex molecules, including pharmaceuticals and agrochemicals, due to its ability to stabilize reactive intermediates. Additionally, it finds application in material science for the development of organic electronic materials, such as OLEDs, where it contributes to improved performance and stability. Its role in asymmetric synthesis is notable, aiding in the production of chiral compounds with high enantiomeric purity.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White to Almost white powder to crystal |
| PURITY | 97.5-100 |
| Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.200 | 10-20 days | ฿1,560.00 |
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| 1.000 | 10-20 days | ฿4,720.00 |
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(3-Bromophenyl)diphenylphosphine Oxide
Widely used as a ligand in transition metal catalysis, particularly in cross-coupling reactions such as Suzuki-Miyaura and Heck reactions, where it enhances the efficiency and selectivity of the process. It is also employed in organic synthesis for the preparation of complex molecules, including pharmaceuticals and agrochemicals, due to its ability to stabilize reactive intermediates. Additionally, it finds application in material science for the development of organic electronic materials, such as OLEDs, where it contributes to improved performance and stability. Its role in asymmetric synthesis is notable, aiding in the production of chiral compounds with high enantiomeric purity.
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