(S)-5-(Chloromethyl)oxazolidin-2-one
95%
- Product Code: 235027
CAS:
169048-83-3
| Molecular Weight: | 135.55 g./mol | Molecular Formula: | C₄H₆ClNO₂ |
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| EC Number: | MDL Number: | ||
| Melting Point: | 86°C | Boiling Point: | |
| Density: | Storage Condition: | 2-8°C |
Product Description:
Used as a chiral auxiliary in asymmetric synthesis, particularly in the preparation of enantiomerically pure pharmaceuticals and fine chemicals. Its structure allows for efficient stereocontrol during carbon-carbon bond-forming reactions. Commonly employed in the Evans aldol reaction, it enables the selective formation of specific stereoisomers, which is critical in drug development. After serving its role in directing stereochemistry, it can be cleaved under mild conditions, leaving the desired chiral product intact. Widely utilized in the synthesis of complex natural products and beta-lactam antibiotics.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 250mg | 10-20 days | ฿600.00 |
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| 1g | 10-20 days | ฿1,590.00 |
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| 5g | 10-20 days | ฿6,350.00 |
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| 25g | 10-20 days | ฿19,280.00 |
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| 100g | 10-20 days | ฿67,080.00 |
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(S)-5-(Chloromethyl)oxazolidin-2-one
Used as a chiral auxiliary in asymmetric synthesis, particularly in the preparation of enantiomerically pure pharmaceuticals and fine chemicals. Its structure allows for efficient stereocontrol during carbon-carbon bond-forming reactions. Commonly employed in the Evans aldol reaction, it enables the selective formation of specific stereoisomers, which is critical in drug development. After serving its role in directing stereochemistry, it can be cleaved under mild conditions, leaving the desired chiral product intact. Widely utilized in the synthesis of complex natural products and beta-lactam antibiotics.
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