4,6-Dichloro-3-iodo-1H-pyrazolo[4,3-c]pyridine

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Reagent Code: #175697
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CAS Number 1658467-36-7

science Other reagents with same CAS 1658467-36-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 313.91 g/mol
Formula C₆H₂Cl₂IN₃
badge Registry Numbers
MDL Number MFCD29921795
thermostat Physical Properties
Boiling Point 465.8±40.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, protected from light, stored in 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 allows for selective modification, making it valuable in creating targeted therapies. It is also employed in research settings to design and optimize new bioactive molecules, especially those aimed at neurological and inflammatory disorders. Due to its halogen substituents, it serves as a versatile building block in cross-coupling reactions, facilitating the formation of complex heterocyclic systems in drug discovery.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,140.00
inventory 250mg
10-20 days ฿1,930.00
inventory 1g
10-20 days ฿4,020.00
inventory 5g
10-20 days ฿11,300.00

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4,6-Dichloro-3-iodo-1H-pyrazolo[4,3-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 modification, making it valuable in creating targeted therapies. It is also employed in research settings to design and optimize new bioactive molecules, especially those aimed at neurological and inflammatory disorders. Due to its halogen substituents, it serves as a versatile building block in cross-coupling reactions, fac

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 modification, making it valuable in creating targeted therapies. It is also employed in research settings to design and optimize new bioactive molecules, especially those aimed at neurological and inflammatory disorders. Due to its halogen substituents, it serves as a versatile building block in cross-coupling reactions, facilitating the formation of complex heterocyclic systems in drug discovery.

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