2-(5-(pyridin-3-yl)-1,3,4-oxadiazol-2-yl)ethanamine

≥95%

Reagent Code: #41750
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CAS Number 933754-48-4

science Other reagents with same CAS 933754-48-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 190.2 g/mol
Formula C₉H₁₀N₄O
badge Registry Numbers
MDL Number MFCD09883765
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry, protected from light

description Product Description

This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of biologically active molecules. Its structure, featuring a pyridine ring and an oxadiazole moiety, makes it a valuable scaffold for developing compounds with potential therapeutic applications. It is often explored for designing drugs targeting various diseases, including cancer, inflammation, and infectious diseases. Additionally, its amine group allows for further functionalization, enabling the creation of derivatives with enhanced pharmacological properties. Researchers also investigate its role in the development of fluorescent probes and imaging agents due to its unique structural characteristics.

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inventory 1g
10-20 days ฿24,570.00

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2-(5-(pyridin-3-yl)-1,3,4-oxadiazol-2-yl)ethanamine
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This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of biologically active molecules. Its structure, featuring a pyridine ring and an oxadiazole moiety, makes it a valuable scaffold for developing compounds with potential therapeutic applications. It is often explored for designing drugs targeting various diseases, including cancer, inflammation, and infectious diseases. Additionally, its amine group allows for further functionalization, enabling

This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of biologically active molecules. Its structure, featuring a pyridine ring and an oxadiazole moiety, makes it a valuable scaffold for developing compounds with potential therapeutic applications. It is often explored for designing drugs targeting various diseases, including cancer, inflammation, and infectious diseases. Additionally, its amine group allows for further functionalization, enabling the creation of derivatives with enhanced pharmacological properties. Researchers also investigate its role in the development of fluorescent probes and imaging agents due to its unique structural characteristics.

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