(R)-tert-Butyl 2-(bromomethyl)morpholine-4-carboxylate
97%
- Product Code: 82960
CAS:
919286-58-1
| Molecular Weight: | 280.16 g./mol | Molecular Formula: | C₁₀H₁₈BrNO₃ |
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| EC Number: | MDL Number: | MFCD20489338 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, store under inert gas |
Product Description:
This chemical is primarily used in organic synthesis as a versatile intermediate for the preparation of complex molecules, particularly in pharmaceutical research. Its structure, featuring a morpholine ring and a bromomethyl group, makes it valuable for constructing nitrogen-containing compounds, which are often found in active pharmaceutical ingredients. The bromomethyl group serves as a reactive site for further functionalization, enabling the introduction of various substituents or the formation of new bonds. Additionally, the tert-butyl ester moiety provides stability and can be selectively removed or transformed under specific conditions, offering flexibility in synthetic routes. This compound is particularly useful in the development of chiral molecules due to its (R)-configuration, which is crucial for producing enantiomerically pure drugs with specific biological activities.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿5,967.00 |
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| 0.250 | 10-20 days | ฿11,232.00 |
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(R)-tert-Butyl 2-(bromomethyl)morpholine-4-carboxylate
This chemical is primarily used in organic synthesis as a versatile intermediate for the preparation of complex molecules, particularly in pharmaceutical research. Its structure, featuring a morpholine ring and a bromomethyl group, makes it valuable for constructing nitrogen-containing compounds, which are often found in active pharmaceutical ingredients. The bromomethyl group serves as a reactive site for further functionalization, enabling the introduction of various substituents or the formation of new bonds. Additionally, the tert-butyl ester moiety provides stability and can be selectively removed or transformed under specific conditions, offering flexibility in synthetic routes. This compound is particularly useful in the development of chiral molecules due to its (R)-configuration, which is crucial for producing enantiomerically pure drugs with specific biological activities.
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