Ethyl 5-(4-nitrophenyl)oxazole-4-carboxylate

98%

Reagent Code: #185348
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CAS Number 72030-87-6

science Other reagents with same CAS 72030-87-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 262.2 g/mol
Formula C₁₂H₁₀N₂O₅
badge Registry Numbers
MDL Number MFCD02179429
inventory_2 Storage & Handling
Storage 2-8°C, dry

description Product Description

Used as an intermediate in the synthesis of biologically active compounds, particularly in the development of pharmaceuticals with potential antitumor and antimicrobial properties. Its structure serves as a key building block in heterocyclic chemistry, enabling the construction of complex oxazole-based molecules. Commonly employed in research settings for designing new drug candidates and in the preparation of fluorescent dyes due to the nitrophenyl group’s electron-withdrawing characteristics. Also utilized in agrochemical research for developing novel pesticides with improved efficacy.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,790.00
inventory 1g
10-20 days ฿5,860.00

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Ethyl 5-(4-nitrophenyl)oxazole-4-carboxylate
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Used as an intermediate in the synthesis of biologically active compounds, particularly in the development of pharmaceuticals with potential antitumor and antimicrobial properties. Its structure serves as a key building block in heterocyclic chemistry, enabling the construction of complex oxazole-based molecules. Commonly employed in research settings for designing new drug candidates and in the preparation of fluorescent dyes due to the nitrophenyl group’s electron-withdrawing characteristics. Also util

Used as an intermediate in the synthesis of biologically active compounds, particularly in the development of pharmaceuticals with potential antitumor and antimicrobial properties. Its structure serves as a key building block in heterocyclic chemistry, enabling the construction of complex oxazole-based molecules. Commonly employed in research settings for designing new drug candidates and in the preparation of fluorescent dyes due to the nitrophenyl group’s electron-withdrawing characteristics. Also utilized in agrochemical research for developing novel pesticides with improved efficacy.

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