Ethyl 5-(4-bromophenyl)-1,3,4-oxadiazole-2-carboxylate

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Reagent Code: #185413
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CAS Number 931760-32-6

science Other reagents with same CAS 931760-32-6

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Weight 297.11 g/mol
Formula C₁₁H₉BrN₂O₃
badge Registry Numbers
MDL Number MFCD14743926
inventory_2 Storage & Handling
Storage 2-8°C, dry

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of bioactive molecules with potential antimicrobial and anti-inflammatory properties. It serves as a building block in medicinal chemistry for constructing heterocyclic compounds that are key in drug discovery. Its bromophenyl and oxadiazole moieties make it valuable for cross-coupling reactions, enabling the creation of diverse chemical libraries for biological screening. Also employed in agrochemical research for designing new active ingredients with enhanced stability and reactivity.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,200.00
inventory 250mg
10-20 days ฿5,500.00
inventory 1g
10-20 days ฿18,690.00

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Ethyl 5-(4-bromophenyl)-1,3,4-oxadiazole-2-carboxylate
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of bioactive molecules with potential antimicrobial and anti-inflammatory properties. It serves as a building block in medicinal chemistry for constructing heterocyclic compounds that are key in drug discovery. Its bromophenyl and oxadiazole moieties make it valuable for cross-coupling reactions, enabling the creation of diverse chemical libraries for biological screening. Also employed in agrochemical rese
Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of bioactive molecules with potential antimicrobial and anti-inflammatory properties. It serves as a building block in medicinal chemistry for constructing heterocyclic compounds that are key in drug discovery. Its bromophenyl and oxadiazole moieties make it valuable for cross-coupling reactions, enabling the creation of diverse chemical libraries for biological screening. Also employed in agrochemical research for designing new active ingredients with enhanced stability and reactivity.
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