ETHYL 5-AMINO-3-CHLOROPYRIDINE-2-CARBOXYLATE

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Reagent Code: #183853
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CAS Number 872355-65-2

science Other reagents with same CAS 872355-65-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 200.62 g/mol
Formula C₈H₉ClN₂O₂
badge Registry Numbers
MDL Number MFCD18250721
inventory_2 Storage & Handling
Storage 2-8°C

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 heterocyclic compounds, which are common in drugs targeting inflammatory diseases, cancer, and central nervous system disorders. The amine and ester functional groups allow for easy modification and coupling reactions, making it valuable in medicinal chemistry for generating compound libraries during drug discovery. Also employed in agrochemical research for designing new active ingredients in crop protection agents.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿9,910.00
inventory 250mg
10-20 days ฿16,870.00
inventory 1g
10-20 days ฿49,290.00

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ETHYL 5-AMINO-3-CHLOROPYRIDINE-2-CARBOXYLATE
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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 heterocyclic compounds, which are common in drugs targeting inflammatory diseases, cancer, and central nervous system disorders. The amine and ester functional groups allow for easy modification and coupling reactions, making it valuable in medicinal chemistry for generating compound libraries dur

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 heterocyclic compounds, which are common in drugs targeting inflammatory diseases, cancer, and central nervous system disorders. The amine and ester functional groups allow for easy modification and coupling reactions, making it valuable in medicinal chemistry for generating compound libraries during drug discovery. Also employed in agrochemical research for designing new active ingredients in crop protection agents.

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