Thieno[2,3-c]pyridin-7(6H)-one

95%

Reagent Code: #242748
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CAS Number 28981-13-7

science Other reagents with same CAS 28981-13-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 151.19 g/mol
Formula C₇H₅NOS
badge Registry Numbers
MDL Number MFCD00122278
thermostat Physical Properties
Melting Point 195 °C
Boiling Point 406.0±45.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.355±0.06 g/cm3(Predicted)
Storage 2-8°C, store away from light, dry seal

description Product Description

Used in pharmaceutical research as a key intermediate in the synthesis of biologically active compounds, particularly kinase inhibitors. Shows potential in the development of anticancer agents due to its structural similarity to purine analogs, enabling interaction with enzyme active sites involved in cell signaling pathways. Also explored for its role in creating novel heterocyclic systems in medicinal chemistry for treating inflammatory diseases and neurological disorders.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,240.00
inventory 250mg
10-20 days ฿2,310.00
inventory 1g
10-20 days ฿4,390.00
inventory 5g
10-20 days ฿18,760.00
inventory 25g
10-20 days ฿79,870.00

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Thieno[2,3-c]pyridin-7(6H)-one
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Used in pharmaceutical research as a key intermediate in the synthesis of biologically active compounds, particularly kinase inhibitors. Shows potential in the development of anticancer agents due to its structural similarity to purine analogs, enabling interaction with enzyme active sites involved in cell signaling pathways. Also explored for its role in creating novel heterocyclic systems in medicinal chemistry for treating inflammatory diseases and neurological disorders.

Used in pharmaceutical research as a key intermediate in the synthesis of biologically active compounds, particularly kinase inhibitors. Shows potential in the development of anticancer agents due to its structural similarity to purine analogs, enabling interaction with enzyme active sites involved in cell signaling pathways. Also explored for its role in creating novel heterocyclic systems in medicinal chemistry for treating inflammatory diseases and neurological disorders.

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