(1-Phenylethyl)(prop-2-en-1-yl)amine

≥95%

Reagent Code: #228178
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CAS Number 66896-61-5

science Other reagents with same CAS 66896-61-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 161.25 g/mol
Formula C₁₁H₁₅N
badge Registry Numbers
MDL Number MFCD12165964
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry, light-proof

description Product Description

Used primarily as an intermediate in organic synthesis, especially in the production of pharmaceuticals and agrochemicals. Its amine functionality and reactive allyl group make it suitable for use in catalytic asymmetric synthesis, where it can serve as a chiral building block. It is also employed in the preparation of bioactive molecules, including potential active ingredients in medicinal chemistry research. Due to the presence of the phenyl and allyl groups, it can participate in various coupling reactions, enabling the construction of complex molecular architectures. Additionally, it may find use in the development of specialty polymers or as a ligand precursor in metal-catalyzed reactions.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿32,010.00
(1-Phenylethyl)(prop-2-en-1-yl)amine
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Used primarily as an intermediate in organic synthesis, especially in the production of pharmaceuticals and agrochemicals. Its amine functionality and reactive allyl group make it suitable for use in catalytic asymmetric synthesis, where it can serve as a chiral building block. It is also employed in the preparation of bioactive molecules, including potential active ingredients in medicinal chemistry research. Due to the presence of the phenyl and allyl groups, it can participate in various coupling reactio
Used primarily as an intermediate in organic synthesis, especially in the production of pharmaceuticals and agrochemicals. Its amine functionality and reactive allyl group make it suitable for use in catalytic asymmetric synthesis, where it can serve as a chiral building block. It is also employed in the preparation of bioactive molecules, including potential active ingredients in medicinal chemistry research. Due to the presence of the phenyl and allyl groups, it can participate in various coupling reactions, enabling the construction of complex molecular architectures. Additionally, it may find use in the development of specialty polymers or as a ligand precursor in metal-catalyzed reactions.
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