N-(1-Phenylethyl)prop-2-yn-1-amine

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Reagent Code: #218145
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CAS Number 56862-34-1

science Other reagents with same CAS 56862-34-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 159.23 g/mol
Formula C₁₁H₁₃N
badge Registry Numbers
MDL Number MFCD03502452
inventory_2 Storage & Handling
Storage 2-8°C, protected from light, stored in inert gas

description Product Description

Used as a building block in organic synthesis, particularly in the preparation of bioactive molecules and pharmaceutical intermediates. Its alkyne and amine functional groups allow for participation in click chemistry reactions, such as copper-catalyzed azide-alkyne cycloaddition (CuAAC), making it valuable in drug discovery and combinatorial chemistry. Also employed in the synthesis of propargyl-containing compounds that show potential in neurological and anticancer research. The presence of a chiral center enables its use in asymmetric synthesis where stereochemistry plays a critical role in biological activity.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,070.00
inventory 250mg
10-20 days ฿3,170.00
inventory 1g
10-20 days ฿8,130.00
inventory 5g
10-20 days ฿26,010.00
N-(1-Phenylethyl)prop-2-yn-1-amine
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Used as a building block in organic synthesis, particularly in the preparation of bioactive molecules and pharmaceutical intermediates. Its alkyne and amine functional groups allow for participation in click chemistry reactions, such as copper-catalyzed azide-alkyne cycloaddition (CuAAC), making it valuable in drug discovery and combinatorial chemistry. Also employed in the synthesis of propargyl-containing compounds that show potential in neurological and anticancer research. The presence of a chiral cente
Used as a building block in organic synthesis, particularly in the preparation of bioactive molecules and pharmaceutical intermediates. Its alkyne and amine functional groups allow for participation in click chemistry reactions, such as copper-catalyzed azide-alkyne cycloaddition (CuAAC), making it valuable in drug discovery and combinatorial chemistry. Also employed in the synthesis of propargyl-containing compounds that show potential in neurological and anticancer research. The presence of a chiral center enables its use in asymmetric synthesis where stereochemistry plays a critical role in biological activity.
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