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

science Other reagents with same CAS 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.

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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

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5-Bromo-2-furaldehyde
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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 functiona

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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