5-Nitrofurfuryl Alcohol

≥98%

Reagent Code: #217529
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CAS Number 2493-04-1

science Other reagents with same CAS 2493-04-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 143.1 g/mol
Formula C₅H₅NO₄
inventory_2 Storage & Handling
Density 1.283g/mL
Storage Room temperature, dry

description Product Description

Used primarily as an intermediate in the synthesis of pharmaceuticals and agrochemicals. It plays a key role in the production of nitrofuran antibiotics, which exhibit broad-spectrum antimicrobial activity. Commonly employed in the development of antifungal and antibacterial agents, especially in veterinary medicine. Also utilized in the preparation of specialty resins and polymers where nitro groups contribute to cross-linking or photo-reactivity. Its alcohol and nitro functional groups allow for diverse chemical modifications, making it valuable in organic synthesis and medicinal chemistry research.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,520.00
inventory 5g
10-20 days ฿7,520.00
inventory 25g
10-20 days ฿26,300.00
5-Nitrofurfuryl Alcohol
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Used primarily as an intermediate in the synthesis of pharmaceuticals and agrochemicals. It plays a key role in the production of nitrofuran antibiotics, which exhibit broad-spectrum antimicrobial activity. Commonly employed in the development of antifungal and antibacterial agents, especially in veterinary medicine. Also utilized in the preparation of specialty resins and polymers where nitro groups contribute to cross-linking or photo-reactivity. Its alcohol and nitro functional groups allow for divers

Used primarily as an intermediate in the synthesis of pharmaceuticals and agrochemicals. It plays a key role in the production of nitrofuran antibiotics, which exhibit broad-spectrum antimicrobial activity. Commonly employed in the development of antifungal and antibacterial agents, especially in veterinary medicine. Also utilized in the preparation of specialty resins and polymers where nitro groups contribute to cross-linking or photo-reactivity. Its alcohol and nitro functional groups allow for diverse chemical modifications, making it valuable in organic synthesis and medicinal chemistry research.

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