(S)-3-(Toluene-4-sulfonyloxy)-pyrrolidine-1-carboxylic acid tert-butyl ester

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Reagent Code: #232627
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CAS Number 371240-55-0

science Other reagents with same CAS 371240-55-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 341.4225 g/mol
Formula C₁₆H₂₃NO₅S
badge Registry Numbers
MDL Number MFCD18252852
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used as an intermediate in the synthesis of biologically active compounds, particularly in the development of pharmaceuticals. Its chiral structure makes it valuable in asymmetric synthesis, where stereochemistry is critical, such as in the production of protease inhibitors or receptor agonists. The tosyl group acts as a leaving group, enabling nucleophilic substitution reactions, while the Boc-protected amine allows for selective deprotection and further functionalization. Commonly employed in medicinal chemistry for constructing complex nitrogen-containing molecules.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,490.00
inventory 1g
10-20 days ฿4,020.00
inventory 5g
10-20 days ฿14,030.00
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(S)-3-(Toluene-4-sulfonyloxy)-pyrrolidine-1-carboxylic acid tert-butyl ester
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Used as an intermediate in the synthesis of biologically active compounds, particularly in the development of pharmaceuticals. Its chiral structure makes it valuable in asymmetric synthesis, where stereochemistry is critical, such as in the production of protease inhibitors or receptor agonists. The tosyl group acts as a leaving group, enabling nucleophilic substitution reactions, while the Boc-protected amine allows for selective deprotection and further functionalization. Commonly employed in medicinal

Used as an intermediate in the synthesis of biologically active compounds, particularly in the development of pharmaceuticals. Its chiral structure makes it valuable in asymmetric synthesis, where stereochemistry is critical, such as in the production of protease inhibitors or receptor agonists. The tosyl group acts as a leaving group, enabling nucleophilic substitution reactions, while the Boc-protected amine allows for selective deprotection and further functionalization. Commonly employed in medicinal chemistry for constructing complex nitrogen-containing molecules.

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