3-(5-Nitro-2-furyl)acrylic Acid

≥97%

Reagent Code: #217656
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CAS Number 6281-23-8

science Other reagents with same CAS 6281-23-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 183.12 g/mol
Formula C₇H₅NO₅
badge Registry Numbers
MDL Number MFCD00143078
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used primarily as an intermediate in organic synthesis, especially in the preparation of heterocyclic compounds and biologically active molecules. Its conjugated structure with a nitrofuran ring makes it valuable in the development of antimicrobial and antifungal agents. It also serves as a building block in the synthesis of pharmaceuticals and agrochemicals, where the nitrofuran moiety contributes to electron-withdrawing properties and reactivity in cyclization reactions. Additionally, derivatives of this compound have been explored for potential applications in medicinal chemistry due to the known biological activity of nitrofuran-based compounds.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿3,010.00
3-(5-Nitro-2-furyl)acrylic Acid
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Used primarily as an intermediate in organic synthesis, especially in the preparation of heterocyclic compounds and biologically active molecules. Its conjugated structure with a nitrofuran ring makes it valuable in the development of antimicrobial and antifungal agents. It also serves as a building block in the synthesis of pharmaceuticals and agrochemicals, where the nitrofuran moiety contributes to electron-withdrawing properties and reactivity in cyclization reactions. Additionally, derivatives of th

Used primarily as an intermediate in organic synthesis, especially in the preparation of heterocyclic compounds and biologically active molecules. Its conjugated structure with a nitrofuran ring makes it valuable in the development of antimicrobial and antifungal agents. It also serves as a building block in the synthesis of pharmaceuticals and agrochemicals, where the nitrofuran moiety contributes to electron-withdrawing properties and reactivity in cyclization reactions. Additionally, derivatives of this compound have been explored for potential applications in medicinal chemistry due to the known biological activity of nitrofuran-based compounds.

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