N-Allyl-N-(1-phenylethyl)prop-2-en-1-amine

95%

Reagent Code: #219943
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CAS Number 92499-04-2

science Other reagents with same CAS 92499-04-2

blur_circular Chemical Specifications

inventory_2 Storage & Handling
Storage 2-8°C, drying away from light

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of functionalized amines and nitrogen-containing heterocycles. Its structure, containing multiple reactive allyl groups and a chiral center, makes it valuable in catalysis and asymmetric synthesis. It can serve as a ligand precursor in metal-catalyzed reactions or as a building block in pharmaceuticals and agrochemicals where amine functionalities are required. The compound's reactivity allows for further transformations such as cyclizations, cross-couplings, or quaternization reactions to form more complex molecular architectures.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,700.00
inventory 250mg
10-20 days ฿4,050.00
inventory 1g
10-20 days ฿13,070.00
N-Allyl-N-(1-phenylethyl)prop-2-en-1-amine
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Used as an intermediate in organic synthesis, particularly in the preparation of functionalized amines and nitrogen-containing heterocycles. Its structure, containing multiple reactive allyl groups and a chiral center, makes it valuable in catalysis and asymmetric synthesis. It can serve as a ligand precursor in metal-catalyzed reactions or as a building block in pharmaceuticals and agrochemicals where amine functionalities are required. The compound's reactivity allows for further transformations such a

Used as an intermediate in organic synthesis, particularly in the preparation of functionalized amines and nitrogen-containing heterocycles. Its structure, containing multiple reactive allyl groups and a chiral center, makes it valuable in catalysis and asymmetric synthesis. It can serve as a ligand precursor in metal-catalyzed reactions or as a building block in pharmaceuticals and agrochemicals where amine functionalities are required. The compound's reactivity allows for further transformations such as cyclizations, cross-couplings, or quaternization reactions to form more complex molecular architectures.

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