5-(2,4-Dichlorophenyl)-3-(pyridin-2-yl)-1,2,4-oxadiazole

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Reagent Code: #130399
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CAS Number 339103-05-8

science Other reagents with same CAS 339103-05-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 292.12 g/mol
Formula C₁₃H₇Cl₂N₃O
badge Registry Numbers
MDL Number MFCD00665263
thermostat Physical Properties
Boiling Point 457.4±55.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.415±0.06 g/cm3(Predicted)
Storage Room temperature, seal, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Shows potential in agrochemical formulations due to its stability and bioactivity, serving as a building block for novel pesticides with improved efficacy against resistant insect strains. Also employed in research settings to design fluorescent probes for studying biological systems, leveraging its electron-withdrawing properties and aromatic structure for sensor applications.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿11,840.00
inventory 1g
10-20 days ฿31,930.00

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5-(2,4-Dichlorophenyl)-3-(pyridin-2-yl)-1,2,4-oxadiazole
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Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Shows potential in agrochemical formulations due to its stability and bioactivity, serving as a building block for novel pesticides with improved efficacy against resistant insect strains. Also employed in research settings to design fluorescent probes for studying biological systems, leveraging its electron-withdrawing properties and aromatic structure for s

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Shows potential in agrochemical formulations due to its stability and bioactivity, serving as a building block for novel pesticides with improved efficacy against resistant insect strains. Also employed in research settings to design fluorescent probes for studying biological systems, leveraging its electron-withdrawing properties and aromatic structure for sensor applications.

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