[bis[3,5-bis(trifluoromethyl)phenyl]-[(2R)-pyrrolidin-2-yl]methoxy]-trimethylsilane

≥95%, ee99%

  • Product Code: 88243
  CAS:    908303-26-4
Molecular Weight: 597.52 g./mol Molecular Formula: C₂₄H₂₃F₁₂NOSi
EC Number: MDL Number: MFCD09750448
Melting Point: Boiling Point: 382.4°C
Density: 1.319g/mL Storage Condition: room temperature, dry
Product Description: This compound is primarily utilized in asymmetric synthesis and catalysis, particularly in organic transformations where high enantioselectivity is required. It serves as a chiral ligand or catalyst in various reactions, such as asymmetric hydrogenation, carbon-carbon bond formation, and other stereoselective processes. Its trifluoromethyl groups enhance electron-withdrawing properties, improving reactivity and selectivity in catalytic systems. Additionally, the trimethylsilane moiety provides stability and facilitates handling in synthetic applications. It is often employed in the pharmaceutical industry for the synthesis of chiral intermediates or active pharmaceutical ingredients (APIs) with high optical purity.
Product Specification:
Test Specification
APPEARANCE White to Beige and Faint Brown to Brown Powder or Crystal or Chunk(s)
Infrared spectrum Conforms to Structure
PURITY 95 100%
e.e 98 100%
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.200 10-20 days ฿4,260.00
+
-
1.000 10-20 days ฿9,500.00
+
-
5.000 10-20 days ฿28,000.00
+
-
[bis[3,5-bis(trifluoromethyl)phenyl]-[(2R)-pyrrolidin-2-yl]methoxy]-trimethylsilane
This compound is primarily utilized in asymmetric synthesis and catalysis, particularly in organic transformations where high enantioselectivity is required. It serves as a chiral ligand or catalyst in various reactions, such as asymmetric hydrogenation, carbon-carbon bond formation, and other stereoselective processes. Its trifluoromethyl groups enhance electron-withdrawing properties, improving reactivity and selectivity in catalytic systems. Additionally, the trimethylsilane moiety provides stability and facilitates handling in synthetic applications. It is often employed in the pharmaceutical industry for the synthesis of chiral intermediates or active pharmaceutical ingredients (APIs) with high optical purity.
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