(E)-3-(5-Nitrofuran-2-yl)acrylaldehyde

98%

Reagent Code: #182452
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CAS Number 52661-56-0

science Other reagents with same CAS 52661-56-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 167.12 g/mol
Formula C₇H₅NO₄
thermostat Physical Properties
Melting Point 284-285°C
Boiling Point 310.7±32.0°C
inventory_2 Storage & Handling
Storage 2-8°C, inert gas atmosphere

description Product Description

Used as an intermediate in the synthesis of nitrofuran antibiotics, which exhibit broad-spectrum antimicrobial activity against bacteria and protozoa. Commonly employed in the development of pharmaceuticals for treating urinary tract infections and gastrointestinal infections. Also serves as a building block in organic synthesis for heterocyclic compounds with potential biological activity. Its α,β-unsaturated aldehyde structure allows for Michael addition reactions, making it valuable in medicinal chemistry research.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿550.00
inventory 250mg
10-20 days ฿1,950.00
inventory 1g
10-20 days ฿7,500.00

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(E)-3-(5-Nitrofuran-2-yl)acrylaldehyde
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Used as an intermediate in the synthesis of nitrofuran antibiotics, which exhibit broad-spectrum antimicrobial activity against bacteria and protozoa. Commonly employed in the development of pharmaceuticals for treating urinary tract infections and gastrointestinal infections. Also serves as a building block in organic synthesis for heterocyclic compounds with potential biological activity. Its α,β-unsaturated aldehyde structure allows for Michael addition reactions, making it valuable in medicinal chemi

Used as an intermediate in the synthesis of nitrofuran antibiotics, which exhibit broad-spectrum antimicrobial activity against bacteria and protozoa. Commonly employed in the development of pharmaceuticals for treating urinary tract infections and gastrointestinal infections. Also serves as a building block in organic synthesis for heterocyclic compounds with potential biological activity. Its α,β-unsaturated aldehyde structure allows for Michael addition reactions, making it valuable in medicinal chemistry research.

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