(5-Nitrofuran-2-yl)methylene diacetate

98%

Reagent Code: #217573
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CAS Number 92-55-7

science Other reagents with same CAS 92-55-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 243.17 g/mol
Formula C₉H₉NO₇
badge Registry Numbers
MDL Number MFCD00003244
thermostat Physical Properties
Melting Point 89-93 °C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used primarily as an intermediate in the synthesis of antimicrobial agents, particularly nitrofuran-based antibiotics. Its structure allows for the introduction of the nitrofuran moiety, which is active against a broad spectrum of bacteria and protozoa. Commonly employed in the preparation of veterinary and pharmaceutical drugs where rapid absorption and metabolic activation are required. Also utilized in research settings to develop new derivatives with enhanced stability and reduced toxicity. The acetyl groups serve as protective functionalities that can be easily removed under mild conditions to reveal the active aldehyde form for further chemical modifications.

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Size Availability Unit Price Quantity
inventory 25g
10-20 days ฿450.00
inventory 100g
10-20 days ฿1,020.00
inventory 500g
10-20 days ฿2,550.00

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(5-Nitrofuran-2-yl)methylene diacetate
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Used primarily as an intermediate in the synthesis of antimicrobial agents, particularly nitrofuran-based antibiotics. Its structure allows for the introduction of the nitrofuran moiety, which is active against a broad spectrum of bacteria and protozoa. Commonly employed in the preparation of veterinary and pharmaceutical drugs where rapid absorption and metabolic activation are required. Also utilized in research settings to develop new derivatives with enhanced stability and reduced toxicity. The acety

Used primarily as an intermediate in the synthesis of antimicrobial agents, particularly nitrofuran-based antibiotics. Its structure allows for the introduction of the nitrofuran moiety, which is active against a broad spectrum of bacteria and protozoa. Commonly employed in the preparation of veterinary and pharmaceutical drugs where rapid absorption and metabolic activation are required. Also utilized in research settings to develop new derivatives with enhanced stability and reduced toxicity. The acetyl groups serve as protective functionalities that can be easily removed under mild conditions to reveal the active aldehyde form for further chemical modifications.

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