6-Chlorothieno[2,3-b]pyridine-2-carbaldehyde

95%

Reagent Code: #142185
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CAS Number 80231-47-6

science Other reagents with same CAS 80231-47-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 197.64 g/mol
Formula C₈H₄ClNOS
badge Registry Numbers
MDL Number MFCD24681130
thermostat Physical Properties
Boiling Point 348.9±37.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.521±0.06 g/cm3(Predicted)
Storage 2-8°C, Sealed, Inert Gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Its structure enables selective binding in biological systems, making it valuable in medicinal chemistry for designing drugs targeting specific signaling pathways. Also employed in the preparation of heterocyclic compounds for research in neurodegenerative diseases and inflammation. Commonly utilized in cross-coupling reactions to build complex molecules in drug discovery and development.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿9,470.00
inventory 250mg
10-20 days ฿16,090.00

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6-Chlorothieno[2,3-b]pyridine-2-carbaldehyde
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Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Its structure enables selective binding in biological systems, making it valuable in medicinal chemistry for designing drugs targeting specific signaling pathways. Also employed in the preparation of heterocyclic compounds for research in neurodegenerative diseases and inflammation. Commonly utilized in cross-coupling reactions to build complex molecules in drug
Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Its structure enables selective binding in biological systems, making it valuable in medicinal chemistry for designing drugs targeting specific signaling pathways. Also employed in the preparation of heterocyclic compounds for research in neurodegenerative diseases and inflammation. Commonly utilized in cross-coupling reactions to build complex molecules in drug discovery and development.
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