2-Amino-5-Bromo-6-Chloropyridin-3-Ol

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Reagent Code: #138851
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CAS Number 1131041-72-9

science Other reagents with same CAS 1131041-72-9

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Weight 223.46 g/mol
Formula C₅H₄BrClN₂O
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Storage Room temperature

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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 medicinal chemistry for creating drug candidates targeting inflammatory diseases and certain cancers. Also employed in agrochemical research for designing novel pesticides due to its halogenated pyridine core, which enhances bioavailability and binding affinity. Commonly utilized in organic synthesis to build complex heterocyclic systems through cross-coupling and nucleophilic substitution reactions.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,750.00
inventory 250mg
10-20 days ฿4,310.00
inventory 1g
10-20 days ฿16,750.00

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2-Amino-5-Bromo-6-Chloropyridin-3-Ol
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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 medicinal chemistry for creating drug candidates targeting inflammatory diseases and certain cancers. Also employed in agrochemical research for designing novel pesticides due to its halogenated pyridine core, which enhances bioavailability and binding affinity. Commonly uti

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 medicinal chemistry for creating drug candidates targeting inflammatory diseases and certain cancers. Also employed in agrochemical research for designing novel pesticides due to its halogenated pyridine core, which enhances bioavailability and binding affinity. Commonly utilized in organic synthesis to build complex heterocyclic systems through cross-coupling and nucleophilic substitution reactions.

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