(S)-tert-Butyl 2,2-dimethyl-4-vinyloxazolidine-3-carboxylate
95%
- Product Code: 38002
CAS:
133625-87-3
| Molecular Weight: | 227.3000 g./mol | Molecular Formula: | C₁₂H₂₁NO₃ |
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| EC Number: | MDL Number: | MFCD09033561 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
This chemical is primarily used in organic synthesis as a chiral auxiliary or building block for the preparation of more complex molecules. Its structure, featuring a vinyl group and an oxazolidine ring, makes it valuable in asymmetric synthesis, particularly in the formation of stereochemically defined compounds. It is often employed in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals where precise control over stereochemistry is crucial. Additionally, the tert-butyl ester group provides stability and can be selectively removed or modified under mild conditions, offering flexibility in synthetic pathways. Its application is particularly notable in the development of chiral catalysts and ligands for enantioselective reactions.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.100 | 10-20 days | ฿8,748.00 |
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(S)-tert-Butyl 2,2-dimethyl-4-vinyloxazolidine-3-carboxylate
This chemical is primarily used in organic synthesis as a chiral auxiliary or building block for the preparation of more complex molecules. Its structure, featuring a vinyl group and an oxazolidine ring, makes it valuable in asymmetric synthesis, particularly in the formation of stereochemically defined compounds. It is often employed in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals where precise control over stereochemistry is crucial. Additionally, the tert-butyl ester group provides stability and can be selectively removed or modified under mild conditions, offering flexibility in synthetic pathways. Its application is particularly notable in the development of chiral catalysts and ligands for enantioselective reactions.
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