4-Bromo-2H-chromen-2-one

≥95%

Reagent Code: #154422
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CAS Number 938-40-9

science Other reagents with same CAS 938-40-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 225.04 g/mol
Formula C₉H₅BrO₂
badge Registry Numbers
MDL Number MFCD00463529
inventory_2 Storage & Handling
Storage 2-8°C, Sealed, Dry, Light-proof, Inert Gas

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals and bioactive compounds, particularly in the development of anticoagulants and anti-inflammatory agents. Its structure serves as a key building block in the preparation of coumarin derivatives, which exhibit a range of biological activities including antimicrobial, anticancer, and antioxidant properties. Commonly employed in organic synthesis for bromine-directed functionalization reactions, enabling the formation of complex heterocyclic systems. Also utilized in research settings to study reaction mechanisms involving electrophilic aromatic substitution and palladium-catalyzed cross-coupling reactions.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿10,000.00
inventory 1g
10-20 days ฿22,000.00
inventory 5g
10-20 days ฿45,000.00

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4-Bromo-2H-chromen-2-one
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Used as an intermediate in the synthesis of pharmaceuticals and bioactive compounds, particularly in the development of anticoagulants and anti-inflammatory agents. Its structure serves as a key building block in the preparation of coumarin derivatives, which exhibit a range of biological activities including antimicrobial, anticancer, and antioxidant properties. Commonly employed in organic synthesis for bromine-directed functionalization reactions, enabling the formation of complex heterocyclic systems

Used as an intermediate in the synthesis of pharmaceuticals and bioactive compounds, particularly in the development of anticoagulants and anti-inflammatory agents. Its structure serves as a key building block in the preparation of coumarin derivatives, which exhibit a range of biological activities including antimicrobial, anticancer, and antioxidant properties. Commonly employed in organic synthesis for bromine-directed functionalization reactions, enabling the formation of complex heterocyclic systems. Also utilized in research settings to study reaction mechanisms involving electrophilic aromatic substitution and palladium-catalyzed cross-coupling reactions.

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