6-Chlorothieno[2,3-b]pyridine

≥95%

Reagent Code: #161986
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CAS Number 62226-18-0

science Other reagents with same CAS 62226-18-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 169.63 g/mol
Formula C₇H₄ClNS
badge Registry Numbers
MDL Number MFCD18253768
thermostat Physical Properties
Boiling Point 269.9±20.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, stored in inert gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors for cancer treatment. Its structure enables selective binding to enzyme targets, making it valuable in drug discovery. Also employed in the preparation of agrochemicals and functional materials due to its electron-rich heterocyclic core. Commonly utilized in cross-coupling reactions to build complex molecules in medicinal chemistry research.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿4,440.00
inventory 100mg
10-20 days ฿15,110.00
inventory 250mg
10-20 days ฿33,470.00
inventory 50mg
10-20 days ฿7,560.00
inventory 1g
10-20 days ฿85,860.00

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6-Chlorothieno[2,3-b]pyridine
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors for cancer treatment. Its structure enables selective binding to enzyme targets, making it valuable in drug discovery. Also employed in the preparation of agrochemicals and functional materials due to its electron-rich heterocyclic core. Commonly utilized in cross-coupling reactions to build complex molecules in medicinal chemistry research.

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors for cancer treatment. Its structure enables selective binding to enzyme targets, making it valuable in drug discovery. Also employed in the preparation of agrochemicals and functional materials due to its electron-rich heterocyclic core. Commonly utilized in cross-coupling reactions to build complex molecules in medicinal chemistry research.

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