5-Bromo-2-furaldehyde

98%

Reagent Code: #143249
label
Alias 5-bromo-2-uranaldehyde; 5-bromo-2-furan formaldehyde, 5-bromofuraldehyde
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CAS Number 1899-24-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 174.98 g/mol
Formula C₅H₃BrO₂
badge Registry Numbers
MDL Number MFCD00159501
thermostat Physical Properties
Melting Point 82-85 °C(lit.)
Boiling Point 112 °C16 mm Hg(lit.)
inventory_2 Storage & Handling
Storage 2~8°C

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of antifungal and antibacterial agents. It serves as a building block in organic reactions due to the reactivity of its aldehyde and bromo functional groups. Commonly employed in cross-coupling reactions such as Suzuki and Heck reactions to form carbon-carbon bonds, enabling the construction of complex furan-containing molecules. Also utilized in the preparation of fluorescent dyes and functional materials where the furan ring acts as a π-conjugated spacer. Its derivatives show potential in medicinal chemistry for designing bioactive compounds with enhanced metabolic stability.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿300.00
inventory 5g
10-20 days ฿590.00
inventory 25g
10-20 days ฿2,120.00
inventory 100g
10-20 days ฿6,990.00
5-Bromo-2-furaldehyde
Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of antifungal and antibacterial agents. It serves as a building block in organic reactions due to the reactivity of its aldehyde and bromo functional groups. Commonly employed in cross-coupling reactions such as Suzuki and Heck reactions to form carbon-carbon bonds, enabling the construction of complex furan-containing molecules. Also utilized in the preparation of fluorescent dyes and functional materials where the furan ring acts as a π-conjugated spacer. Its derivatives show potential in medicinal chemistry for designing bioactive compounds with enhanced metabolic stability.
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