(R)-tert-Butyl 4-(3-bromoprop-1-en-1-yl)-2,2-dimethyloxazolidine-3-carboxylate[R-(E)]-
97%
- Product Code: 228776
CAS:
142573-55-5
| Molecular Weight: | 320.22 g./mol | Molecular Formula: | C₁₃H₂₂BrNO₃ |
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| EC Number: | MDL Number: | MFCD26406788 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature |
Product Description:
Used as a chiral building block in the synthesis of complex organic molecules, particularly in pharmaceuticals where stereochemistry is critical. Its structure allows for selective introduction of functional groups in asymmetric synthesis. The bromoalkene moiety serves as a versatile handle for cross-coupling reactions such as Suzuki or Heck reactions, enabling the construction of carbon-carbon bonds. The oxazolidine ring acts as a protecting group for amines and also directs stereoselectivity in subsequent transformations. Commonly employed in the development of bioactive compounds, including potential drug candidates in medicinal chemistry research.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
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| 0.100 | 10-20 days | $281.15 |
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| 0.250 | 10-20 days | $567.98 |
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| 0.500 | 10-20 days | $947.27 |
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(R)-tert-Butyl 4-(3-bromoprop-1-en-1-yl)-2,2-dimethyloxazolidine-3-carboxylate[R-(E)]-
Used as a chiral building block in the synthesis of complex organic molecules, particularly in pharmaceuticals where stereochemistry is critical. Its structure allows for selective introduction of functional groups in asymmetric synthesis. The bromoalkene moiety serves as a versatile handle for cross-coupling reactions such as Suzuki or Heck reactions, enabling the construction of carbon-carbon bonds. The oxazolidine ring acts as a protecting group for amines and also directs stereoselectivity in subsequent transformations. Commonly employed in the development of bioactive compounds, including potential drug candidates in medicinal chemistry research.
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