2-Amino-4-bromopyridin-3-ol hydrobromide

95%

Reagent Code: #137490
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CAS Number 114414-17-4

science Other reagents with same CAS 114414-17-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 269.92 g/mol
Formula C₅H₆Br₂N₂O
badge Registry Numbers
MDL Number MFCD09842810
inventory_2 Storage & Handling
Storage 2-8°C, inflatable

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for creating compounds with potential anticancer, antiviral, or anti-inflammatory activity. Also employed in the preparation of heterocyclic compounds used in agrochemicals and organic electronic materials due to its electron-rich aromatic system and halogen handle for cross-coupling reactions.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿390.00
inventory 250mg
10-20 days ฿870.00
inventory 1g
10-20 days ฿2,690.00

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2-Amino-4-bromopyridin-3-ol hydrobromide
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for creating compounds with potential anticancer, antiviral, or anti-inflammatory activity. Also employed in the preparation of heterocyclic compounds used in agrochemicals and organic electronic materials due to its electron-rich aromatic system and halogen handle

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for creating compounds with potential anticancer, antiviral, or anti-inflammatory activity. Also employed in the preparation of heterocyclic compounds used in agrochemicals and organic electronic materials due to its electron-rich aromatic system and halogen handle for cross-coupling reactions.

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