Methyl 7-bromo-1-chloroisoquinoline-3-carboxylate

95%

Reagent Code: #203773
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CAS Number 1597882-11-5

science Other reagents with same CAS 1597882-11-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 300.5358 g/mol
Formula C₁₁H₇BrClNO₂
thermostat Physical Properties
Boiling Point 436.1±40.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.644±0.06 g/cm3(Predicted)
Storage 2-8°C

description Product Description

Used in pharmaceutical research as an intermediate for synthesizing bioactive isoquinoline derivatives. Its halogenated structure allows for cross-coupling reactions, making it valuable in developing potential anticancer, antimicrobial, and anti-inflammatory agents. Commonly employed in medicinal chemistry to build complex heterocyclic systems through palladium-catalyzed reactions. Also utilized in the preparation of kinase inhibitors and receptor modulators during drug discovery.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿19,200.00
250mg
10-20 days ฿31,680.00
1g
10-20 days ฿60,800.00
Methyl 7-bromo-1-chloroisoquinoline-3-carboxylate
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Used in pharmaceutical research as an intermediate for synthesizing bioactive isoquinoline derivatives. Its halogenated structure allows for cross-coupling reactions, making it valuable in developing potential anticancer, antimicrobial, and anti-inflammatory agents. Commonly employed in medicinal chemistry to build complex heterocyclic systems through palladium-catalyzed reactions. Also utilized in the preparation of kinase inhibitors and receptor modulators during drug discovery.

Used in pharmaceutical research as an intermediate for synthesizing bioactive isoquinoline derivatives. Its halogenated structure allows for cross-coupling reactions, making it valuable in developing potential anticancer, antimicrobial, and anti-inflammatory agents. Commonly employed in medicinal chemistry to build complex heterocyclic systems through palladium-catalyzed reactions. Also utilized in the preparation of kinase inhibitors and receptor modulators during drug discovery.

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