Methyl 3-amino-5-methoxyisonicotinate

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Reagent Code: #130588
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CAS Number 82673-74-3

science Other reagents with same CAS 82673-74-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 182.18 g/mol
Formula C₈H₁₀N₂O₃
badge Registry Numbers
MDL Number MFCD20715877
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 other bioactive molecules. Its structure supports the construction of nitrogen-containing heterocycles, which are common in drugs targeting inflammatory diseases, cancer, and central nervous system disorders. The amine and ester functional groups allow for easy modification, making it valuable in medicinal chemistry for structure-activity relationship (SAR) studies. It is also employed in the preparation of agrochemicals and functional materials due to its reactivity and stability in multi-step syntheses.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿5,250.00
inventory 250mg
10-20 days ฿8,930.00

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Methyl 3-amino-5-methoxyisonicotinate
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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 supports the construction of nitrogen-containing heterocycles, which are common in drugs targeting inflammatory diseases, cancer, and central nervous system disorders. The amine and ester functional groups allow for easy modification, making it valuable in medicinal chemistry for structure-activity relationship (SAR) studies. It is also employed

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure supports the construction of nitrogen-containing heterocycles, which are common in drugs targeting inflammatory diseases, cancer, and central nervous system disorders. The amine and ester functional groups allow for easy modification, making it valuable in medicinal chemistry for structure-activity relationship (SAR) studies. It is also employed in the preparation of agrochemicals and functional materials due to its reactivity and stability in multi-step syntheses.

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