(2R,4S)-1-Benzyl 2-methyl 4-aminopyrrolidine-1,2-dicarboxylate hydrochloride

≥95%

Reagent Code: #36499
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CAS Number 489446-77-7

science Other reagents with same CAS 489446-77-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 314.77 g/mol
Formula C₁₄H₁₉ClN₂O₄
badge Registry Numbers
MDL Number MFCD11101170
inventory_2 Storage & Handling
Storage 2-8°C, store under inert gas

description Product Description

This compound is primarily utilized in pharmaceutical research and development, particularly in the synthesis of chiral intermediates for drug candidates. Its structure, featuring both amino and ester functional groups, makes it valuable in the creation of biologically active molecules, especially those targeting the central nervous system. It is often employed in the preparation of compounds with potential therapeutic effects, such as enzyme inhibitors or receptor modulators. Additionally, its chiral nature allows for the production of enantiomerically pure substances, which is critical in the development of drugs with specific efficacy and reduced side effects. The hydrochloride salt form enhances its stability and solubility, facilitating its use in various experimental and manufacturing processes.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿2,313.00
inventory 100mg
10-20 days ฿1,152.00

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(2R,4S)-1-Benzyl 2-methyl 4-aminopyrrolidine-1,2-dicarboxylate hydrochloride
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This compound is primarily utilized in pharmaceutical research and development, particularly in the synthesis of chiral intermediates for drug candidates. Its structure, featuring both amino and ester functional groups, makes it valuable in the creation of biologically active molecules, especially those targeting the central nervous system. It is often employed in the preparation of compounds with potential therapeutic effects, such as enzyme inhibitors or receptor modulators. Additionally, its chiral na

This compound is primarily utilized in pharmaceutical research and development, particularly in the synthesis of chiral intermediates for drug candidates. Its structure, featuring both amino and ester functional groups, makes it valuable in the creation of biologically active molecules, especially those targeting the central nervous system. It is often employed in the preparation of compounds with potential therapeutic effects, such as enzyme inhibitors or receptor modulators. Additionally, its chiral nature allows for the production of enantiomerically pure substances, which is critical in the development of drugs with specific efficacy and reduced side effects. The hydrochloride salt form enhances its stability and solubility, facilitating its use in various experimental and manufacturing processes.

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