2,2'-Isopropylidenebis[(4S)-4-tert-butyl-2-oxazoline]
95%
- Product Code: 126741
Alias:
(S,S)-(-)-2,2'-Isopropylidenebis(4-tert-butyl-2-oxazoline)
CAS:
131833-93-7
| Molecular Weight: | 294.43 g./mol | Molecular Formula: | C₁₇H₃₀N₂O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00192243 | |
| Melting Point: | 89-91 °C(lit.) | Boiling Point: | |
| Density: | Storage Condition: | room temperature |
Product Description:
This chemical is primarily utilized as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where enantioselectivity is crucial. It is often employed in transition metal-catalyzed processes, such as hydrogenation, to produce chiral molecules with high optical purity. Its rigid structure and stereochemical properties make it effective in controlling the spatial arrangement of reactants, leading to the formation of specific enantiomers. This is especially valuable in the pharmaceutical industry for synthesizing enantiomerically pure drugs, where the biological activity can be highly dependent on the correct chiral form. Additionally, it finds use in academic research for developing new methodologies in organic synthesis and exploring stereochemical outcomes in complex reactions.
Product Specification:
| Test | Specification |
|---|---|
| Appearance | White To Off-White Solid |
| Purity (%) | 94.5-100 |
| Infrared Spectrum | Conforms To Structure |
| NMR | Conforms To Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿1,650.00 |
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| 0.250 | 10-20 days | ฿2,490.00 |
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2,2'-Isopropylidenebis[(4S)-4-tert-butyl-2-oxazoline]
This chemical is primarily utilized as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where enantioselectivity is crucial. It is often employed in transition metal-catalyzed processes, such as hydrogenation, to produce chiral molecules with high optical purity. Its rigid structure and stereochemical properties make it effective in controlling the spatial arrangement of reactants, leading to the formation of specific enantiomers. This is especially valuable in the pharmaceutical industry for synthesizing enantiomerically pure drugs, where the biological activity can be highly dependent on the correct chiral form. Additionally, it finds use in academic research for developing new methodologies in organic synthesis and exploring stereochemical outcomes in complex reactions.
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