(2S,4S)-tert-Butyl 4-amino-2-(hydroxymethyl)pyrrolidine-1-carboxylate

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Reagent Code: #36583
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CAS Number 922139-40-0

science Other reagents with same CAS 922139-40-0

blur_circular Chemical Specifications

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Weight 216.2774 g/mol
Formula C₁₀H₂₀N₂O₃
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MDL Number MFCD08704520
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description Product Description

This compound is primarily used in the synthesis of pharmaceutical intermediates, particularly in the development of bioactive molecules and drug candidates. Its structure, featuring both amino and hydroxymethyl groups, makes it a versatile building block for constructing complex molecules, especially in the field of medicinal chemistry. It is often employed in the production of protease inhibitors, which are critical in treating diseases such as HIV and hepatitis C. Additionally, its chiral centers allow for the creation of enantiomerically pure compounds, enhancing the specificity and efficacy of the resulting drugs. The tert-butyl group provides steric protection during synthetic processes, ensuring selective reactions and improved yields.

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inventory 100mg
10-20 days ฿5,427.00

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(2S,4S)-tert-Butyl 4-amino-2-(hydroxymethyl)pyrrolidine-1-carboxylate
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This compound is primarily used in the synthesis of pharmaceutical intermediates, particularly in the development of bioactive molecules and drug candidates. Its structure, featuring both amino and hydroxymethyl groups, makes it a versatile building block for constructing complex molecules, especially in the field of medicinal chemistry. It is often employed in the production of protease inhibitors, which are critical in treating diseases such as HIV and hepatitis C. Additionally, its chiral centers allo

This compound is primarily used in the synthesis of pharmaceutical intermediates, particularly in the development of bioactive molecules and drug candidates. Its structure, featuring both amino and hydroxymethyl groups, makes it a versatile building block for constructing complex molecules, especially in the field of medicinal chemistry. It is often employed in the production of protease inhibitors, which are critical in treating diseases such as HIV and hepatitis C. Additionally, its chiral centers allow for the creation of enantiomerically pure compounds, enhancing the specificity and efficacy of the resulting drugs. The tert-butyl group provides steric protection during synthetic processes, ensuring selective reactions and improved yields.

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