N-(Propargyloxy)phthalimide

≥98%

Reagent Code: #124822
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CAS Number 4616-63-1

science Other reagents with same CAS 4616-63-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 201.18 g/mol
Formula C₁₁H₇NO₃
badge Registry Numbers
MDL Number MFCD00005890
thermostat Physical Properties
Melting Point 138-142°C
inventory_2 Storage & Handling
Storage room temperature

description Product Description

N-(Propargyloxy)phthalimide is primarily utilized in organic synthesis as a versatile building block for the preparation of various heterocyclic compounds. Its propargyloxy group enables it to participate in click chemistry reactions, particularly copper-catalyzed azide-alkyne cycloaddition (CuAAC), which is widely employed in the development of pharmaceuticals, polymers, and bioconjugates. Additionally, it serves as a key intermediate in the synthesis of biologically active molecules, including potential drug candidates, due to its ability to introduce phthalimide and propargyl functionalities into target structures. Its applications also extend to materials science, where it contributes to the creation of functionalized polymers and advanced materials with tailored properties.

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Test Parameter Specification
Appearance White To Pale Yellow Solid
Purity 97.5-100
Melting Point (°C) 135-155

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Size Availability Unit Price Quantity
inventory 200mg
10-20 days ฿960.00
inventory 1g
10-20 days ฿2,250.00

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N-(Propargyloxy)phthalimide
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N-(Propargyloxy)phthalimide is primarily utilized in organic synthesis as a versatile building block for the preparation of various heterocyclic compounds. Its propargyloxy group enables it to participate in click chemistry reactions, particularly copper-catalyzed azide-alkyne cycloaddition (CuAAC), which is widely employed in the development of pharmaceuticals, polymers, and bioconjugates. Additionally, it serves as a key intermediate in the synthesis of biologically active molecules, including potentia

N-(Propargyloxy)phthalimide is primarily utilized in organic synthesis as a versatile building block for the preparation of various heterocyclic compounds. Its propargyloxy group enables it to participate in click chemistry reactions, particularly copper-catalyzed azide-alkyne cycloaddition (CuAAC), which is widely employed in the development of pharmaceuticals, polymers, and bioconjugates. Additionally, it serves as a key intermediate in the synthesis of biologically active molecules, including potential drug candidates, due to its ability to introduce phthalimide and propargyl functionalities into target structures. Its applications also extend to materials science, where it contributes to the creation of functionalized polymers and advanced materials with tailored properties.

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