Ethyl 2-(3-nitrobenzylidene)acetoacetate

97%

Reagent Code: #184793
label
Alias (E)-2-(3-nitrobenzylidene)-3-oxobutyrate Ethyl ester
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CAS Number 39562-16-8

science Other reagents with same CAS 39562-16-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 263.25 g/mol
Formula C₁₃H₁₃NO₅
badge Registry Numbers
MDL Number MFCD00713511
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. It serves as a building block in the formation of heterocyclic compounds due to its α,β-unsaturated carbonyl structure, which readily participates in Michael addition and cycloaddition reactions. Commonly employed in the synthesis of nitro-substituted pyrazoles and other nitrogen-containing rings with biological activity. Also utilized in research for developing fluorescent dyes and photoactive materials owing to its conjugated system and electron-withdrawing nitro group.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,190.00
inventory 5g
10-20 days ฿3,230.00
inventory 25g
10-20 days ฿8,090.00
inventory 100g
10-20 days ฿28,600.00

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Ethyl 2-(3-nitrobenzylidene)acetoacetate
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Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. It serves as a building block in the formation of heterocyclic compounds due to its α,β-unsaturated carbonyl structure, which readily participates in Michael addition and cycloaddition reactions. Commonly employed in the synthesis of nitro-substituted pyrazoles and other nitrogen-containing rings with biological activity. Also utilized in research for developing fluorescent dyes and photoac

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. It serves as a building block in the formation of heterocyclic compounds due to its α,β-unsaturated carbonyl structure, which readily participates in Michael addition and cycloaddition reactions. Commonly employed in the synthesis of nitro-substituted pyrazoles and other nitrogen-containing rings with biological activity. Also utilized in research for developing fluorescent dyes and photoactive materials owing to its conjugated system and electron-withdrawing nitro group.

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