4-Bromo-1-methyl-1H-pyrrole-2-carboxylic acid

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Reagent Code: #146633
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CAS Number 875160-43-3

science Other reagents with same CAS 875160-43-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 204.02 g/mol
Formula C₆H₆BrNO₂
thermostat Physical Properties
Melting Point 136-138°C
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 bioactive molecules with antimicrobial or antitumor properties. Its structure serves as a building block in heterocyclic chemistry, enabling the construction of complex pyrrole derivatives. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to the bromine atom facilitating further functionalization via cross-coupling reactions. Also utilized in the preparation of functional materials and ligands for catalysis.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,870.00
inventory 5g
10-20 days ฿8,400.00
inventory 10g
10-20 days ฿16,710.00
inventory 25g
10-20 days ฿36,290.00

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4-Bromo-1-methyl-1H-pyrrole-2-carboxylic acid
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Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of bioactive molecules with antimicrobial or antitumor properties. Its structure serves as a building block in heterocyclic chemistry, enabling the construction of complex pyrrole derivatives. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to the bromine atom facilitating further functionalization via cross-coupling reactions. Also utilized in the

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of bioactive molecules with antimicrobial or antitumor properties. Its structure serves as a building block in heterocyclic chemistry, enabling the construction of complex pyrrole derivatives. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to the bromine atom facilitating further functionalization via cross-coupling reactions. Also utilized in the preparation of functional materials and ligands for catalysis.

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