Methyl 2-amino-4-(pyridin-2-yl)thiophene-3-carboxylate

≥95%

Reagent Code: #205739
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CAS Number 1019521-30-2

science Other reagents with same CAS 1019521-30-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 234.27 g/mol
Formula C₁₁H₁₀N₂O₂S
badge Registry Numbers
MDL Number MFCD11136556
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other biologically active molecules. Its structure supports the formation of heterocyclic systems commonly found 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 studies. Also employed in the preparation of agrochemicals and functional materials due to its stable aromatic and heterocyclic framework.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿9,260.00
inventory 250mg
10-20 days ฿15,730.00
Methyl 2-amino-4-(pyridin-2-yl)thiophene-3-carboxylate
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Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other biologically active molecules. Its structure supports the formation of heterocyclic systems commonly found 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 studies. Also employed in the prepar
Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other biologically active molecules. Its structure supports the formation of heterocyclic systems commonly found 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 studies. Also employed in the preparation of agrochemicals and functional materials due to its stable aromatic and heterocyclic framework.
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