4-Bromo-5-chlorothiophene-2-carboxylic acid

96%

Reagent Code: #148756
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CAS Number 60729-37-5

science Other reagents with same CAS 60729-37-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 241.49 g/mol
Formula C₅H₂BrClO₂S
badge Registry Numbers
MDL Number MFCD00847582
inventory_2 Storage & Handling
Storage 2-8°C, protected from light, stored in inert gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of thiophene-based bioactive molecules. Its functional groups, including bromine, chlorine, and carboxylic acid, allow for selective modifications such as nucleophilic substitutions and palladium- or copper-catalyzed cross-coupling reactions for carbon-carbon bond formation, making it valuable in constructing complex organic compounds in fewer steps. Commonly employed in the preparation of antifungal, antibacterial, and anti-inflammatory agents. Also utilized in the manufacture of specialty polymers and electronic materials due to the electron-rich nature of the thiophene ring.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,940.00
inventory 250mg
10-20 days ฿7,370.00
inventory 1g
10-20 days ฿23,960.00

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4-Bromo-5-chlorothiophene-2-carboxylic acid
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Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of thiophene-based bioactive molecules. Its functional groups, including bromine, chlorine, and carboxylic acid, allow for selective modifications such as nucleophilic substitutions and palladium- or copper-catalyzed cross-coupling reactions for carbon-carbon bond formation, making it valuable in constructing complex organic compounds in fewer steps. Commonly employed in the preparation of an

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of thiophene-based bioactive molecules. Its functional groups, including bromine, chlorine, and carboxylic acid, allow for selective modifications such as nucleophilic substitutions and palladium- or copper-catalyzed cross-coupling reactions for carbon-carbon bond formation, making it valuable in constructing complex organic compounds in fewer steps. Commonly employed in the preparation of antifungal, antibacterial, and anti-inflammatory agents. Also utilized in the manufacture of specialty polymers and electronic materials due to the electron-rich nature of the thiophene ring.

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