5-Bromo-4-methoxynicotinaldehyde

98%

Reagent Code: #145275
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CAS Number 1289161-72-3

science Other reagents with same CAS 1289161-72-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 216.03 g/mol
Formula C₇H₆BrNO₂
badge Registry Numbers
MDL Number MFCD28740848
thermostat Physical Properties
Boiling Point 296.8±35.0°C
inventory_2 Storage & Handling
Storage 2-8°C, inert gas atmosphere

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of nicotinamide-based drugs and kinase inhibitors. Its aldehyde and bromo functionalities allow for selective chemical modifications, making it valuable in constructing complex heterocyclic systems. Commonly employed in cross-coupling reactions such as Suzuki and Heck reactions to build biaryl structures found in bioactive molecules. Also utilized in agrochemical research for designing novel pesticides with improved efficacy and selectivity. Its methoxy and bromo groups enhance reactivity and guide regioselective substitutions during multi-step syntheses.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿1,850.00
inventory 250mg
10-20 days ฿5,600.00

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5-Bromo-4-methoxynicotinaldehyde
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of nicotinamide-based drugs and kinase inhibitors. Its aldehyde and bromo functionalities allow for selective chemical modifications, making it valuable in constructing complex heterocyclic systems. Commonly employed in cross-coupling reactions such as Suzuki and Heck reactions to build biaryl structures found in bioactive molecules. Also utilized in agrochemical research for designing novel pesticides with im

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of nicotinamide-based drugs and kinase inhibitors. Its aldehyde and bromo functionalities allow for selective chemical modifications, making it valuable in constructing complex heterocyclic systems. Commonly employed in cross-coupling reactions such as Suzuki and Heck reactions to build biaryl structures found in bioactive molecules. Also utilized in agrochemical research for designing novel pesticides with improved efficacy and selectivity. Its methoxy and bromo groups enhance reactivity and guide regioselective substitutions during multi-step syntheses.

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