3-Iodo-7-methoxy-1H-pyrrolo[2,3-c]pyridine

≥95%

Reagent Code: #200649
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CAS Number 1190316-96-1

science Other reagents with same CAS 1190316-96-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 274.06 g/mol
Formula C₈H₇IN₂O
badge Registry Numbers
MDL Number MFCD12963282
thermostat Physical Properties
Boiling Point 385.3 °C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, protected from light, dry, sealed

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 allows for selective functionalization, making it valuable in medicinal chemistry for creating targeted therapies. Commonly employed in cross-coupling reactions to introduce aryl or heteroaryl groups, enabling the construction of complex molecules with biological activity. Also utilized in research settings to develop new neuroprotective agents and treatments for inflammatory diseases.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,110.00
inventory 250mg
10-20 days ฿5,260.00
inventory 1g
10-20 days ฿19,730.00

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3-Iodo-7-methoxy-1H-pyrrolo[2,3-c]pyridine
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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 allows for selective functionalization, making it valuable in medicinal chemistry for creating targeted therapies. Commonly employed in cross-coupling reactions to introduce aryl or heteroaryl groups, enabling the construction of complex molecules with biological activity. Also utilized in research settings to develop new neuroprotective agents

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for creating targeted therapies. Commonly employed in cross-coupling reactions to introduce aryl or heteroaryl groups, enabling the construction of complex molecules with biological activity. Also utilized in research settings to develop new neuroprotective agents and treatments for inflammatory diseases.

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