5-Nitrofurfural

98%

Reagent Code: #217014
label
Alias 5-nitrofuran-2-formaldehyde; 5-nitro-2-furan formaldehyde; 5-nitrofuran formaldehyde
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CAS Number 698-63-5

science Other reagents with same CAS 698-63-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 141.08 g/mol
Formula C₅H₃NO₄
badge Registry Numbers
MDL Number MFCD00003230
inventory_2 Storage & Handling
Storage Room temperature, sealed

description Product Description

Used primarily as an intermediate in organic synthesis, especially in the production of pharmaceuticals and agrochemicals. It serves as a building block for heterocyclic compounds due to the reactivity of the aldehyde and nitro groups. Commonly employed in the synthesis of nitrofuran antibiotics, which exhibit broad-spectrum antimicrobial activity. Also utilized in the development of dyes and functional materials where electron-withdrawing groups enhance photochemical properties. Its derivatives are explored in medicinal chemistry for antiparasitic and antifungal applications.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿260.00
inventory 5g
10-20 days ฿460.00
inventory 25g
10-20 days ฿1,630.00
inventory 500g
10-20 days ฿21,850.00
inventory 100g
10-20 days ฿5,560.00
5-Nitrofurfural
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Used primarily as an intermediate in organic synthesis, especially in the production of pharmaceuticals and agrochemicals. It serves as a building block for heterocyclic compounds due to the reactivity of the aldehyde and nitro groups. Commonly employed in the synthesis of nitrofuran antibiotics, which exhibit broad-spectrum antimicrobial activity. Also utilized in the development of dyes and functional materials where electron-withdrawing groups enhance photochemical properties. Its derivatives are explore
Used primarily as an intermediate in organic synthesis, especially in the production of pharmaceuticals and agrochemicals. It serves as a building block for heterocyclic compounds due to the reactivity of the aldehyde and nitro groups. Commonly employed in the synthesis of nitrofuran antibiotics, which exhibit broad-spectrum antimicrobial activity. Also utilized in the development of dyes and functional materials where electron-withdrawing groups enhance photochemical properties. Its derivatives are explored in medicinal chemistry for antiparasitic and antifungal applications.
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