PEPPSI-SIPr catalyst
98%
- Product Code: 68331
Alias:
(1,3-bis(2,6-diisopropylphenyl)imidazolylidene)(3-chloropyridyl)palladium(II) dichloride
CAS:
927706-57-8
| Molecular Weight: | 681.47 g./mol | Molecular Formula: | C₃₂H₄₂Cl₃N₃Pd |
|---|---|---|---|
| EC Number: | MDL Number: | ||
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| Density: | Storage Condition: | room temperature |
Product Description:
The PEPPSI-SIPr catalyst is widely used in organic synthesis, particularly in cross-coupling reactions. It is highly effective in facilitating C-C bond formation, making it valuable in the synthesis of complex organic molecules. Its application extends to the production of pharmaceuticals, agrochemicals, and fine chemicals, where precise and efficient coupling reactions are essential. The catalyst is also utilized in the preparation of heterocyclic compounds, which are crucial in drug development. Additionally, its stability and versatility make it suitable for use in challenging reaction conditions, including those involving sensitive functional groups. Its role in enabling efficient and selective transformations underscores its importance in modern synthetic chemistry.
Product Specification:
| Test | Specification |
|---|---|
| Appearance | White to Yellow, powder |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿1,900.00 |
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| 1.000 | 10-20 days | ฿7,450.00 |
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PEPPSI-SIPr catalyst
The PEPPSI-SIPr catalyst is widely used in organic synthesis, particularly in cross-coupling reactions. It is highly effective in facilitating C-C bond formation, making it valuable in the synthesis of complex organic molecules. Its application extends to the production of pharmaceuticals, agrochemicals, and fine chemicals, where precise and efficient coupling reactions are essential. The catalyst is also utilized in the preparation of heterocyclic compounds, which are crucial in drug development. Additionally, its stability and versatility make it suitable for use in challenging reaction conditions, including those involving sensitive functional groups. Its role in enabling efficient and selective transformations underscores its importance in modern synthetic chemistry.
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