3-(3-(Bromomethyl)phenyl)-5-methyl-1,2,4-oxadiazole

98%

Reagent Code: #140969
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CAS Number 253273-90-4

science Other reagents with same CAS 253273-90-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 253.1 g/mol
Formula C₁₀H₉BrN₂O
badge Registry Numbers
MDL Number MFCD07368547
thermostat Physical Properties
Melting Point 71 °C
Boiling Point 369.4±44.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.491±0.06 g/cm3(Predicted)
Storage 2-8°C, Inert Gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of bioactive molecules targeting central nervous system disorders. Its bromomethyl group allows for easy functionalization, enabling coupling reactions with nucleophiles to form ether, thioether, or amine derivatives. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to the stability and metabolic resistance of the 1,2,4-oxadiazole ring. Also utilized in the preparation of fluorescent probes and labeled compounds for biochemical assays, where the oxadiazole moiety acts as a fluorophore or bioisostere. Shows potential in agrochemical research for designing novel pesticides with improved selectivity and environmental profile.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿8,890.00
inventory 1g
10-20 days ฿40,730.00
3-(3-(Bromomethyl)phenyl)-5-methyl-1,2,4-oxadiazole
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Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of bioactive molecules targeting central nervous system disorders. Its bromomethyl group allows for easy functionalization, enabling coupling reactions with nucleophiles to form ether, thioether, or amine derivatives. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to the stability and metabolic resistance of the 1,2,4-oxadiazole ring. Also utilized in th

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of bioactive molecules targeting central nervous system disorders. Its bromomethyl group allows for easy functionalization, enabling coupling reactions with nucleophiles to form ether, thioether, or amine derivatives. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to the stability and metabolic resistance of the 1,2,4-oxadiazole ring. Also utilized in the preparation of fluorescent probes and labeled compounds for biochemical assays, where the oxadiazole moiety acts as a fluorophore or bioisostere. Shows potential in agrochemical research for designing novel pesticides with improved selectivity and environmental profile.

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