4-Bromofuran-3-carboxylic acid

98%

Reagent Code: #130092
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CAS Number 116779-79-4

science Other reagents with same CAS 116779-79-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 190.98 g/mol
Formula C₅H₃BrO₃
badge Registry Numbers
MDL Number MFCD32738839
thermostat Physical Properties
Boiling Point 275.8±25.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.891±0.06 g/cm3(Predicted)
Storage 2-8°C, sealed, dry

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its structure allows for further functionalization, making it valuable in constructing heterocyclic compounds. Commonly employed in cross-coupling reactions such as Suzuki and Heck reactions to form carbon-carbon bonds. Also utilized in the development of bioactive molecules and functional materials due to the presence of both bromine and carboxylic acid groups, which offer multiple reaction sites.

Available Sizes & Pricing

Size Availability Unit Price Quantity
250mg
10-20 days ฿20,650.00
100mg
10-20 days ฿10,330.00
4-Bromofuran-3-carboxylic acid
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Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its structure allows for further functionalization, making it valuable in constructing heterocyclic compounds. Commonly employed in cross-coupling reactions such as Suzuki and Heck reactions to form carbon-carbon bonds. Also utilized in the development of bioactive molecules and functional materials due to the presence of both bromine and carboxylic acid groups, which offer multiple reactio

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its structure allows for further functionalization, making it valuable in constructing heterocyclic compounds. Commonly employed in cross-coupling reactions such as Suzuki and Heck reactions to form carbon-carbon bonds. Also utilized in the development of bioactive molecules and functional materials due to the presence of both bromine and carboxylic acid groups, which offer multiple reaction sites.

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