6-Bromo-3-methoxypicolinaldehyde

97%

Reagent Code: #146696
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CAS Number 945954-95-0

science Other reagents with same CAS 945954-95-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 216.03 g/mol
Formula C₇H₆BrNO₂
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 kinase inhibitors and other biologically active compounds. Its structure allows for selective functionalization, making it valuable in constructing complex heterocyclic systems. Commonly employed in cross-coupling reactions such as Suzuki and Heck reactions to build carbon-carbon bonds in drug discovery. Also utilized in agrochemical research for designing novel pesticides and herbicides due to its reactivity and ability to introduce bromine and aldehyde functionalities in target molecules.

Available Sizes & Pricing

Size Availability Unit Price Quantity
25mg
10-20 days ฿850.00
100mg
10-20 days ฿1,720.00
1g
10-20 days ฿10,300.00
250mg
10-20 days ฿2,960.00
6-Bromo-3-methoxypicolinaldehyde
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other biologically active compounds. Its structure allows for selective functionalization, making it valuable in constructing complex heterocyclic systems. Commonly employed in cross-coupling reactions such as Suzuki and Heck reactions to build carbon-carbon bonds in drug discovery. Also utilized in agrochemical research for designing novel pesticides and herbicides due to its reactivi

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other biologically active compounds. Its structure allows for selective functionalization, making it valuable in constructing complex heterocyclic systems. Commonly employed in cross-coupling reactions such as Suzuki and Heck reactions to build carbon-carbon bonds in drug discovery. Also utilized in agrochemical research for designing novel pesticides and herbicides due to its reactivity and ability to introduce bromine and aldehyde functionalities in target molecules.

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