1-[(tert-Butoxy)carbonyl]-3-ethylpyrrolidine-3-carboxylic acid

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Reagent Code: #39583
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CAS Number 1158751-03-1

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Weight 243.2994 g/mol
Formula C₁₂H₂₁NO₄
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This chemical is primarily used as an intermediate in the synthesis of more complex organic compounds, particularly in pharmaceutical research. It plays a key role in the development of active pharmaceutical ingredients (APIs) due to its functional groups, which allow for further modifications. The tert-butoxycarbonyl (Boc) group acts as a protecting group for amines, enabling selective reactions in multi-step synthetic processes. The compound is often utilized in the preparation of pyrrolidine-based molecules, which are common scaffolds in drug discovery for their potential therapeutic applications. Its ethyl and carboxylic acid groups provide additional sites for chemical transformations, making it a versatile building block in medicinal chemistry.

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inventory 100mg
10-20 days ฿3,942.00

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1-[(tert-Butoxy)carbonyl]-3-ethylpyrrolidine-3-carboxylic acid
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This chemical is primarily used as an intermediate in the synthesis of more complex organic compounds, particularly in pharmaceutical research. It plays a key role in the development of active pharmaceutical ingredients (APIs) due to its functional groups, which allow for further modifications. The tert-butoxycarbonyl (Boc) group acts as a protecting group for amines, enabling selective reactions in multi-step synthetic processes. The compound is often utilized in the preparation of pyrrolidine-based mol

This chemical is primarily used as an intermediate in the synthesis of more complex organic compounds, particularly in pharmaceutical research. It plays a key role in the development of active pharmaceutical ingredients (APIs) due to its functional groups, which allow for further modifications. The tert-butoxycarbonyl (Boc) group acts as a protecting group for amines, enabling selective reactions in multi-step synthetic processes. The compound is often utilized in the preparation of pyrrolidine-based molecules, which are common scaffolds in drug discovery for their potential therapeutic applications. Its ethyl and carboxylic acid groups provide additional sites for chemical transformations, making it a versatile building block in medicinal chemistry.

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