CYCLOPENTADIENYL(P-CYMENE)RUTHENIUM (II) HEXAFLUOROPHOSPHATE, MIN
98%
- Product Code: 61143
CAS:
147831-75-2
| Molecular Weight: | 445.35 g./mol | Molecular Formula: | C₁₀H₁₄C₅H₅F₆PRu |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD06798307 | |
| Melting Point: | 83-84 °C | Boiling Point: | |
| Density: | Storage Condition: | Room temperature, dry, sealed, inflated |
Product Description:
Cyclopentadienyl(p-cymene)ruthenium (II) hexafluorophosphate is widely used in organic synthesis, particularly as a catalyst in various chemical reactions. It is highly effective in promoting transfer hydrogenation, a process that reduces organic compounds by transferring hydrogen atoms from a donor molecule. This makes it valuable in the production of pharmaceuticals and fine chemicals. Additionally, it is utilized in C-H activation reactions, enabling the functionalization of otherwise inert carbon-hydrogen bonds, which is crucial for creating complex molecular structures. Its stability and efficiency also make it a preferred choice in asymmetric synthesis, where it helps produce chiral compounds with high enantioselectivity.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿9,009.00 |
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| 1.000 | 10-20 days | ฿27,261.00 |
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CYCLOPENTADIENYL(P-CYMENE)RUTHENIUM (II) HEXAFLUOROPHOSPHATE, MIN
Cyclopentadienyl(p-cymene)ruthenium (II) hexafluorophosphate is widely used in organic synthesis, particularly as a catalyst in various chemical reactions. It is highly effective in promoting transfer hydrogenation, a process that reduces organic compounds by transferring hydrogen atoms from a donor molecule. This makes it valuable in the production of pharmaceuticals and fine chemicals. Additionally, it is utilized in C-H activation reactions, enabling the functionalization of otherwise inert carbon-hydrogen bonds, which is crucial for creating complex molecular structures. Its stability and efficiency also make it a preferred choice in asymmetric synthesis, where it helps produce chiral compounds with high enantioselectivity.
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