(S)-()-4-Isopropyl-3-propionyl-2-oxazolidinone
98%
- Product Code: 60210
Alias:
(S)-3-Propionyl-4-isopropyl-2-oxazolidinone
CAS:
77877-19-1
| Molecular Weight: | 185.22 g./mol | Molecular Formula: | C₉H₁₅NO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00043401 | |
| Melting Point: | Boiling Point: | 102-106 °C0.75 mm Hg(lit.) | |
| Density: | 1.094 g/mL at 25 °C(lit.) | Storage Condition: | 2~8°C |
Product Description:
This chemical is widely used as a chiral auxiliary in asymmetric synthesis, particularly in the preparation of enantiomerically pure compounds. It is highly effective in controlling stereochemistry during reactions, such as aldol additions, alkylations, and Diels-Alder reactions. Its rigid structure and ability to form stable complexes with metal catalysts make it a valuable tool in organic synthesis for producing pharmaceuticals and fine chemicals with high enantiomeric purity. Additionally, it is employed in the synthesis of complex natural products and bioactive molecules, where precise stereocontrol is critical.
Product Specification:
| Test | Specification |
|---|---|
| Optical RotationDegrees C8.7 CH2Cl2 | 91.0 97.0 |
| PurityGC | 98 100% |
| REFRACTIVE INDEX N20D | 1.463-1.467 |
| SPECIFIC GRAVITY 2020C | 1.097-1.1 |
| SPECIFIC ROTATION A20DNEAT | 87-91 |
| APPEARANCE | COLORLESS LIQUID |
| INFRARED SPECTRUM | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿2,900.00 |
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| 5.000 | 10-20 days | ฿12,750.00 |
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(S)-()-4-Isopropyl-3-propionyl-2-oxazolidinone
This chemical is widely used as a chiral auxiliary in asymmetric synthesis, particularly in the preparation of enantiomerically pure compounds. It is highly effective in controlling stereochemistry during reactions, such as aldol additions, alkylations, and Diels-Alder reactions. Its rigid structure and ability to form stable complexes with metal catalysts make it a valuable tool in organic synthesis for producing pharmaceuticals and fine chemicals with high enantiomeric purity. Additionally, it is employed in the synthesis of complex natural products and bioactive molecules, where precise stereocontrol is critical.
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