tert-Butyl 3-bromo-4-oxopyrrolidine-1-carboxylate

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Reagent Code: #45220
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CAS Number 885278-03-5

science Other reagents with same CAS 885278-03-5

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Weight 264.1300 g/mol
Formula C₉H₁₄BrNO₃
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MDL Number MFCD06738526
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This compound is primarily utilized in organic synthesis as a versatile intermediate for the construction of complex molecules, particularly in pharmaceutical research. It serves as a key building block in the development of pyrrolidine-based compounds, which are often explored for their biological activities. The bromo and carbonyl functional groups make it a valuable substrate for further chemical modifications, such as nucleophilic substitution or coupling reactions, enabling the synthesis of diverse heterocyclic structures. Its tert-butyl carboxylate group provides stability and ease of handling during synthetic processes, making it a preferred choice in medicinal chemistry for drug discovery and development.

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inventory 1g
10-20 days ฿29,745.00

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tert-Butyl 3-bromo-4-oxopyrrolidine-1-carboxylate
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This compound is primarily utilized in organic synthesis as a versatile intermediate for the construction of complex molecules, particularly in pharmaceutical research. It serves as a key building block in the development of pyrrolidine-based compounds, which are often explored for their biological activities. The bromo and carbonyl functional groups make it a valuable substrate for further chemical modifications, such as nucleophilic substitution or coupling reactions, enabling the synthesis of diverse het
This compound is primarily utilized in organic synthesis as a versatile intermediate for the construction of complex molecules, particularly in pharmaceutical research. It serves as a key building block in the development of pyrrolidine-based compounds, which are often explored for their biological activities. The bromo and carbonyl functional groups make it a valuable substrate for further chemical modifications, such as nucleophilic substitution or coupling reactions, enabling the synthesis of diverse heterocyclic structures. Its tert-butyl carboxylate group provides stability and ease of handling during synthetic processes, making it a preferred choice in medicinal chemistry for drug discovery and development.
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