(2S,4S)-1-Benzyl 2-methyl 4-((tert-butoxycarbonyl)amino)pyrrolidine-1,2-dicarboxylate

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Reagent Code: #70872
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CAS Number 168263-80-7

science Other reagents with same CAS 168263-80-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 378.42 g/mol
Formula C₁₉H₂₆N₂O₆
badge Registry Numbers
MDL Number MFCD29920507
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

This compound is primarily utilized in the synthesis of complex organic molecules, particularly in pharmaceutical research. It serves as a key intermediate in the development of peptidomimetics and other bioactive compounds. The presence of the tert-butoxycarbonyl (Boc) protecting group allows for selective reactions, making it valuable in multi-step synthetic processes. Its chiral structure is crucial for producing enantiomerically pure substances, which is essential in drug development to ensure efficacy and reduce side effects. Additionally, it is employed in the preparation of proline derivatives, which are significant in designing enzyme inhibitors and receptor modulators.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,250.00
inventory 250mg
10-20 days ฿3,780.00
inventory 1g
10-20 days ฿7,785.00

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(2S,4S)-1-Benzyl 2-methyl 4-((tert-butoxycarbonyl)amino)pyrrolidine-1,2-dicarboxylate
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This compound is primarily utilized in the synthesis of complex organic molecules, particularly in pharmaceutical research. It serves as a key intermediate in the development of peptidomimetics and other bioactive compounds. The presence of the tert-butoxycarbonyl (Boc) protecting group allows for selective reactions, making it valuable in multi-step synthetic processes. Its chiral structure is crucial for producing enantiomerically pure substances, which is essential in drug development to ensure effica

This compound is primarily utilized in the synthesis of complex organic molecules, particularly in pharmaceutical research. It serves as a key intermediate in the development of peptidomimetics and other bioactive compounds. The presence of the tert-butoxycarbonyl (Boc) protecting group allows for selective reactions, making it valuable in multi-step synthetic processes. Its chiral structure is crucial for producing enantiomerically pure substances, which is essential in drug development to ensure efficacy and reduce side effects. Additionally, it is employed in the preparation of proline derivatives, which are significant in designing enzyme inhibitors and receptor modulators.

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