Ethyl 4-bromo-6-chloronicotinate

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Reagent Code: #183709
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CAS Number 1807221-07-3

science Other reagents with same CAS 1807221-07-3

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Weight 264.50 g/mol
Formula C₈H₇BrClNO₂
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MDL Number MFCD26520840
inventory_2 Storage & Handling
Storage 2-8°C, stored in inert gas

description Product Description

Used as a key intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the development of herbicides and plant growth regulators. Its halogenated structure allows for selective cross-coupling reactions, making it valuable in building complex heterocyclic systems. Commonly employed in research settings for modifying nicotinate-based scaffolds to enhance biological activity. Also utilized in the preparation of kinase inhibitors and other bioactive molecules due to its reactivity with nucleophiles and transition-metal catalysts.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,790.00
inventory 250mg
10-20 days ฿7,460.00
inventory 1g
10-20 days ฿20,490.00

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Ethyl 4-bromo-6-chloronicotinate
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Used as a key intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the development of herbicides and plant growth regulators. Its halogenated structure allows for selective cross-coupling reactions, making it valuable in building complex heterocyclic systems. Commonly employed in research settings for modifying nicotinate-based scaffolds to enhance biological activity. Also utilized in the preparation of kinase inhibitors and other bioactive molecules due to its reactivity

Used as a key intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the development of herbicides and plant growth regulators. Its halogenated structure allows for selective cross-coupling reactions, making it valuable in building complex heterocyclic systems. Commonly employed in research settings for modifying nicotinate-based scaffolds to enhance biological activity. Also utilized in the preparation of kinase inhibitors and other bioactive molecules due to its reactivity with nucleophiles and transition-metal catalysts.

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