3-Benzyl-1-(tert-butoxycarbonyl)pyrrolidine-3-carboxylicacid

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Reagent Code: #155030
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CAS Number 1316757-61-5

science Other reagents with same CAS 1316757-61-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 305.37 g/mol
Formula C₁₇H₂₃NO₄
badge Registry Numbers
MDL Number MFCD18273562
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of protease inhibitors and other bioactive molecules. Its structure supports the construction of complex organic molecules by providing a chiral scaffold that can be further modified in multi-step reactions. Commonly employed in medicinal chemistry for drug discovery programs targeting viral infections and metabolic disorders. The Boc-protected amine and carboxylic acid functionalities allow for selective derivatization, making it valuable in solid-phase and solution-phase peptide-like synthesis.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿16,030.00

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3-Benzyl-1-(tert-butoxycarbonyl)pyrrolidine-3-carboxylicacid
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Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of protease inhibitors and other bioactive molecules. Its structure supports the construction of complex organic molecules by providing a chiral scaffold that can be further modified in multi-step reactions. Commonly employed in medicinal chemistry for drug discovery programs targeting viral infections and metabolic disorders. The Boc-protected amine and carboxylic acid functionalities allow for selec

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of protease inhibitors and other bioactive molecules. Its structure supports the construction of complex organic molecules by providing a chiral scaffold that can be further modified in multi-step reactions. Commonly employed in medicinal chemistry for drug discovery programs targeting viral infections and metabolic disorders. The Boc-protected amine and carboxylic acid functionalities allow for selective derivatization, making it valuable in solid-phase and solution-phase peptide-like synthesis.

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