N-(p-Toluenesulfonyl)-2-pyrroline

98%

Reagent Code: #218274
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CAS Number 130719-30-1

science Other reagents with same CAS 130719-30-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 223.29142 g/mol
Formula C₁₁H₁₃NO₂S
badge Registry Numbers
MDL Number MFCD27943234
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in organic synthesis, particularly in the preparation of pyrrolidine and pyrrolidine-based compounds which are common structural motifs in pharmaceuticals and natural products. Its reactivity allows for selective ring-opening and functionalization reactions, making it valuable in the development of bioactive molecules. Commonly employed in asymmetric synthesis and cyclization processes to construct nitrogen-containing heterocycles. Also utilized in the synthesis of protease inhibitors and other medicinal agents where controlled stereochemistry is required.

Available Sizes & Pricing

Size Availability Unit Price Quantity
250mg
10-20 days ฿10,370.00
1g
10-20 days ฿30,960.00
N-(p-Toluenesulfonyl)-2-pyrroline
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Used as a key intermediate in organic synthesis, particularly in the preparation of pyrrolidine and pyrrolidine-based compounds which are common structural motifs in pharmaceuticals and natural products. Its reactivity allows for selective ring-opening and functionalization reactions, making it valuable in the development of bioactive molecules. Commonly employed in asymmetric synthesis and cyclization processes to construct nitrogen-containing heterocycles. Also utilized in the synthesis of protease inh

Used as a key intermediate in organic synthesis, particularly in the preparation of pyrrolidine and pyrrolidine-based compounds which are common structural motifs in pharmaceuticals and natural products. Its reactivity allows for selective ring-opening and functionalization reactions, making it valuable in the development of bioactive molecules. Commonly employed in asymmetric synthesis and cyclization processes to construct nitrogen-containing heterocycles. Also utilized in the synthesis of protease inhibitors and other medicinal agents where controlled stereochemistry is required.

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