4,5-Dibromo-1H-pyrrole-2-carboxylic acid

96%

Reagent Code: #178589
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CAS Number 34649-21-3

science Other reagents with same CAS 34649-21-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 268.9 g/mol
Formula C₅H₃Br₂NO₂
badge Registry Numbers
MDL Number MFCD01348229
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used in organic synthesis as a building block for pharmaceuticals and bioactive compounds. Its structure supports the development of nitrogen-containing heterocycles, which are common in drug discovery. Commonly employed in the preparation of pyrrole-based derivatives with potential antimicrobial, antifungal, or anticancer properties. Also utilized in materials science for designing functionalized polymers and electronic materials due to the electron-rich nature of the pyrrole ring. The bromine substituents allow further modification through cross-coupling reactions, enabling diverse chemical transformations.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,300.00
inventory 250mg
10-20 days ฿8,570.00

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4,5-Dibromo-1H-pyrrole-2-carboxylic acid
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Used in organic synthesis as a building block for pharmaceuticals and bioactive compounds. Its structure supports the development of nitrogen-containing heterocycles, which are common in drug discovery. Commonly employed in the preparation of pyrrole-based derivatives with potential antimicrobial, antifungal, or anticancer properties. Also utilized in materials science for designing functionalized polymers and electronic materials due to the electron-rich nature of the pyrrole ring. The bromine substitue

Used in organic synthesis as a building block for pharmaceuticals and bioactive compounds. Its structure supports the development of nitrogen-containing heterocycles, which are common in drug discovery. Commonly employed in the preparation of pyrrole-based derivatives with potential antimicrobial, antifungal, or anticancer properties. Also utilized in materials science for designing functionalized polymers and electronic materials due to the electron-rich nature of the pyrrole ring. The bromine substituents allow further modification through cross-coupling reactions, enabling diverse chemical transformations.

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