N-(p-Toluenesulfonyl)-3-pyrroline

98%

Reagent Code: #217687
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CAS Number 16851-72-2

science Other reagents with same CAS 16851-72-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 223.29 g/mol
Formula C₁₁H₁₃NO₂S
badge Registry Numbers
MDL Number MFCD01321189
thermostat Physical Properties
Melting Point 125-128°C
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a key intermediate in organic synthesis, particularly in the preparation of pyrrolidine and pyrroline derivatives which are common structural motifs in pharmaceuticals and natural products. It serves as a protected form of 3-pyrroline, enabling selective reactions at other functional sites without interference from the reactive imine group. Its tosyl protection group enhances stability and facilitates purification, making it valuable in multi-step syntheses of bioactive molecules, including drug candidates targeting neurological and cardiovascular conditions. Also employed in asymmetric synthesis and cyclization reactions to construct nitrogen-containing heterocycles.

Available Sizes & Pricing

Size Availability Unit Price Quantity
250mg
10-20 days ฿700.00
1g
10-20 days ฿1,940.00
5g
10-20 days ฿5,000.00
N-(p-Toluenesulfonyl)-3-pyrroline
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Used as a key intermediate in organic synthesis, particularly in the preparation of pyrrolidine and pyrroline derivatives which are common structural motifs in pharmaceuticals and natural products. It serves as a protected form of 3-pyrroline, enabling selective reactions at other functional sites without interference from the reactive imine group. Its tosyl protection group enhances stability and facilitates purification, making it valuable in multi-step syntheses of bioactive molecules, including drug

Used as a key intermediate in organic synthesis, particularly in the preparation of pyrrolidine and pyrroline derivatives which are common structural motifs in pharmaceuticals and natural products. It serves as a protected form of 3-pyrroline, enabling selective reactions at other functional sites without interference from the reactive imine group. Its tosyl protection group enhances stability and facilitates purification, making it valuable in multi-step syntheses of bioactive molecules, including drug candidates targeting neurological and cardiovascular conditions. Also employed in asymmetric synthesis and cyclization reactions to construct nitrogen-containing heterocycles.

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