1-Boc-3-cyanopyrrolidine

98%

Reagent Code: #143480
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Alias 1-Boc-3-Cyanopyrrolidine
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CAS Number 476493-40-0

science Other reagents with same CAS 476493-40-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 196.25 g/mol
Formula C₁₀H₁₆N₂O₂
badge Registry Numbers
MDL Number MFCD03001709
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of protease inhibitors and other biologically active compounds. Its protected amine group (Boc) and reactive nitrile functionality allow selective reactions in multi-step organic syntheses. Commonly employed in the preparation of antidiabetic agents, such as DPP-4 inhibitors, due to the pyrrolidine scaffold’s role in mimicking peptide structures. The compound enables efficient chirality transfer and is valued in medicinal chemistry for building complex molecules with high stereochemical control.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿600.00
inventory 1g
10-20 days ฿1,120.00
inventory 5g
10-20 days ฿4,640.00
inventory 25g
10-20 days ฿16,500.00

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1-Boc-3-cyanopyrrolidine
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of protease inhibitors and other biologically active compounds. Its protected amine group (Boc) and reactive nitrile functionality allow selective reactions in multi-step organic syntheses. Commonly employed in the preparation of antidiabetic agents, such as DPP-4 inhibitors, due to the pyrrolidine scaffold’s role in mimicking peptide structures. The compound enables efficient chirality transfer and is valued

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of protease inhibitors and other biologically active compounds. Its protected amine group (Boc) and reactive nitrile functionality allow selective reactions in multi-step organic syntheses. Commonly employed in the preparation of antidiabetic agents, such as DPP-4 inhibitors, due to the pyrrolidine scaffold’s role in mimicking peptide structures. The compound enables efficient chirality transfer and is valued in medicinal chemistry for building complex molecules with high stereochemical control.

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