6-Hydroxypicolinamide

97%

Reagent Code: #195634
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CAS Number 89640-67-5

science Other reagents with same CAS 89640-67-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 138.12 g/mol
Formula C₆H₆N₂O₂
badge Registry Numbers
MDL Number MFCD11506698
inventory_2 Storage & Handling
Storage Store in an inert gas at room temperature

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry due to its ability to form stable complexes with metal ions, enhancing its utility in designing bioactive molecules. Also employed in the preparation of heterocyclic compounds for agrochemicals and functional materials. Its hydroxyl and amide groups allow for diverse derivatization, making it valuable in structure-activity relationship studies.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,450.00
inventory 250mg
10-20 days ฿2,450.00
inventory 1g
10-20 days ฿6,600.00
inventory 5g
10-20 days ฿23,070.00

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6-Hydroxypicolinamide
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry due to its ability to form stable complexes with metal ions, enhancing its utility in designing bioactive molecules. Also employed in the preparation of heterocyclic compounds for agrochemicals and functional materials. Its hydroxyl and amide groups allow for diverse derivatization, making it valuable in structure-a

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry due to its ability to form stable complexes with metal ions, enhancing its utility in designing bioactive molecules. Also employed in the preparation of heterocyclic compounds for agrochemicals and functional materials. Its hydroxyl and amide groups allow for diverse derivatization, making it valuable in structure-activity relationship studies.

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