(1-Allylpyrrolidin-2-yl)methanamine

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Reagent Code: #135598
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CAS Number 26116-13-2

science Other reagents with same CAS 26116-13-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 138.21 g/mol
Formula C₈H₁₄N₂
thermostat Physical Properties
Boiling Point 194.6±13.0°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used primarily as a building block in organic synthesis, this compound serves in the development of pharmaceuticals and biologically active molecules. Its amine and allyl functional groups allow for versatile reactivity, enabling use in catalysis, ligand design, and the preparation of nitrogen-containing heterocycles. It is also employed in research settings for the synthesis of novel psychoactive substances, making it relevant in forensic chemistry and drug metabolism studies. Due to its reactivity, it is valuable in forming amide bonds, undergoing alkylation, or participating in multistep synthetic routes for medicinal chemistry applications.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿2,000.00
inventory 100mg
10-20 days ฿4,990.00
inventory 250mg
10-20 days ฿7,970.00

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(1-Allylpyrrolidin-2-yl)methanamine
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Used primarily as a building block in organic synthesis, this compound serves in the development of pharmaceuticals and biologically active molecules. Its amine and allyl functional groups allow for versatile reactivity, enabling use in catalysis, ligand design, and the preparation of nitrogen-containing heterocycles. It is also employed in research settings for the synthesis of novel psychoactive substances, making it relevant in forensic chemistry and drug metabolism studies. Due to its reactivity, it

Used primarily as a building block in organic synthesis, this compound serves in the development of pharmaceuticals and biologically active molecules. Its amine and allyl functional groups allow for versatile reactivity, enabling use in catalysis, ligand design, and the preparation of nitrogen-containing heterocycles. It is also employed in research settings for the synthesis of novel psychoactive substances, making it relevant in forensic chemistry and drug metabolism studies. Due to its reactivity, it is valuable in forming amide bonds, undergoing alkylation, or participating in multistep synthetic routes for medicinal chemistry applications.

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