R-1-Boc-3-cyanopyrrolidine

96%

Reagent Code: #229840
label
Alias (R)-1-Boc-3-cyanopyrrolidine
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CAS Number 132945-76-7

science Other reagents with same CAS 132945-76-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 196.25 g/mol
Formula C₁₀H₁₆N₂O₂
badge Registry Numbers
MDL Number MFCD05863904
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) requiring high enantiomeric purity. Its protected amine and nitrile functional groups allow for selective transformations, making it valuable in multi-step organic syntheses. Commonly employed in the preparation of protease inhibitors and other bioactive molecules where the pyrrolidine scaffold is essential. The Boc group enables easy deprotection under mild acidic conditions, facilitating further coupling reactions in peptide-like structures or heterocycle formation. Widely utilized in medicinal chemistry for structure-activity relationship (SAR) studies.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,160.00
inventory 1g
10-20 days ฿4,050.00

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R-1-Boc-3-cyanopyrrolidine
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) requiring high enantiomeric purity. Its protected amine and nitrile functional groups allow for selective transformations, making it valuable in multi-step organic syntheses. Commonly employed in the preparation of protease inhibitors and other bioactive molecules where the pyrrolidine scaffold is essential. The Boc group enables easy deprotection under mild aci

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) requiring high enantiomeric purity. Its protected amine and nitrile functional groups allow for selective transformations, making it valuable in multi-step organic syntheses. Commonly employed in the preparation of protease inhibitors and other bioactive molecules where the pyrrolidine scaffold is essential. The Boc group enables easy deprotection under mild acidic conditions, facilitating further coupling reactions in peptide-like structures or heterocycle formation. Widely utilized in medicinal chemistry for structure-activity relationship (SAR) studies.

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