3-Amino-5-fluoropyridin-2-ol

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Reagent Code: #131280
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CAS Number 1257069-38-7

science Other reagents with same CAS 1257069-38-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 128.1 g/mol
Formula C₅H₅FN₂O
badge Registry Numbers
MDL Number MFCD19216201
inventory_2 Storage & Handling
Storage 2-8°C, light-proof, inert gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and antiviral agents. Its structure supports the formation of biologically active compounds that target specific enzyme pathways. Commonly employed in medicinal chemistry for constructing heterocyclic systems found in drug candidates. Also utilized in agrochemicals for designing novel pesticides due to its ability to enhance binding selectivity. Its amino and hydroxyl functional groups allow for easy modification, making it valuable in combinatorial chemistry and high-throughput screening.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿9,640.00
inventory 250mg
10-20 days ฿16,370.00

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3-Amino-5-fluoropyridin-2-ol
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and antiviral agents. Its structure supports the formation of biologically active compounds that target specific enzyme pathways. Commonly employed in medicinal chemistry for constructing heterocyclic systems found in drug candidates. Also utilized in agrochemicals for designing novel pesticides due to its ability to enhance binding selectivity. Its amino and hydroxyl functional groups all

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and antiviral agents. Its structure supports the formation of biologically active compounds that target specific enzyme pathways. Commonly employed in medicinal chemistry for constructing heterocyclic systems found in drug candidates. Also utilized in agrochemicals for designing novel pesticides due to its ability to enhance binding selectivity. Its amino and hydroxyl functional groups allow for easy modification, making it valuable in combinatorial chemistry and high-throughput screening.

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