(R,R)-(-)-N,N'-Bis(3,5-di-tert-butylsalicylidene)-1,2-cyclohexanediaminomanganese(III) chloride
≥98%
- Product Code: 64453
Alias:
(R,R)-Jacobsen catalyst; Jacobsen catalyst
CAS:
138124-32-0
| Molecular Weight: | 635.20 g./mol | Molecular Formula: | C₃₆H₅₂ClMnN₂O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD02101664 | |
| Melting Point: | 330-332 °C | Boiling Point: | |
| Density: | Storage Condition: | room temperature |
Product Description:
This chemical is widely used as a highly effective catalyst in asymmetric epoxidation reactions, particularly for the conversion of alkenes into epoxides. Its application is crucial in the synthesis of chiral epoxides, which are valuable intermediates in the production of pharmaceuticals, agrochemicals, and fine chemicals. The catalyst’s enantioselectivity allows for the creation of optically active compounds, which are essential in the development of drugs with specific biological activities. Additionally, it is employed in organic synthesis to achieve high yields and stereochemical control, making it a preferred choice in industrial and academic research settings. Its robustness and efficiency under mild reaction conditions further enhance its utility in complex chemical transformations.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿3,250.00 |
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(R,R)-(-)-N,N'-Bis(3,5-di-tert-butylsalicylidene)-1,2-cyclohexanediaminomanganese(III) chloride
This chemical is widely used as a highly effective catalyst in asymmetric epoxidation reactions, particularly for the conversion of alkenes into epoxides. Its application is crucial in the synthesis of chiral epoxides, which are valuable intermediates in the production of pharmaceuticals, agrochemicals, and fine chemicals. The catalyst’s enantioselectivity allows for the creation of optically active compounds, which are essential in the development of drugs with specific biological activities. Additionally, it is employed in organic synthesis to achieve high yields and stereochemical control, making it a preferred choice in industrial and academic research settings. Its robustness and efficiency under mild reaction conditions further enhance its utility in complex chemical transformations.
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