()-2,2'-Isopropylidenebis[(4R)-4-phenyl-2-oxazoline]
96%
- Product Code: 126740
Alias:
(R,R)-2,2'-Isopropylidene bis(4-phenyl-2-oxazoline)
CAS:
150529-93-4
| Molecular Weight: | 334.41 g./mol | Molecular Formula: | C₂₁H₂₂N₂O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00192244 | |
| Melting Point: | 56-58 °C(lit.) | Boiling Point: | |
| Density: | Storage Condition: | -20℃ |
Product Description:
This chemical is primarily used as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where enantioselectivity is crucial. It is often employed in metal-catalyzed transformations, such as hydrogenation, cyclopropanation, and carbon-carbon bond-forming reactions, to produce optically active compounds. Its rigid structure and chiral centers make it effective in controlling the stereochemistry of the reaction products. Additionally, it finds applications in the synthesis of pharmaceuticals and fine chemicals, where high enantiomeric purity is essential. Its stability and ability to form complexes with various transition metals further enhance its utility in organic synthesis.
Product Specification:
| Test | Specification |
|---|---|
| Purity (GC) | 95.5-100 |
| Specific Rotation | 155-165 |
| Specific Rotation | 155-165 |
| Appearance | Light-Yellow To Yellow Liquid Or Solid |
| Infrared Spectrum | Conforms To Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | $78.01 |
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()-2,2'-Isopropylidenebis[(4R)-4-phenyl-2-oxazoline]
This chemical is primarily used as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where enantioselectivity is crucial. It is often employed in metal-catalyzed transformations, such as hydrogenation, cyclopropanation, and carbon-carbon bond-forming reactions, to produce optically active compounds. Its rigid structure and chiral centers make it effective in controlling the stereochemistry of the reaction products. Additionally, it finds applications in the synthesis of pharmaceuticals and fine chemicals, where high enantiomeric purity is essential. Its stability and ability to form complexes with various transition metals further enhance its utility in organic synthesis.
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