1H-Pyrrolo[2,3-c]pyridine-4-carbonitrile

≥95%

Reagent Code: #195638
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CAS Number 1190319-59-5

science Other reagents with same CAS 1190319-59-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 143.15 g/mol
Formula C₈H₅N₃
badge Registry Numbers
MDL Number MFCD12963363
inventory_2 Storage & Handling
Storage 2-8°C, dry seal

description Product Description

Used in pharmaceutical research as a key intermediate in the synthesis of kinase inhibitors, particularly for targeted cancer therapies. Its structure supports the development of compounds with high selectivity toward specific signaling pathways involved in tumor growth. Also explored in the design of anti-inflammatory agents due to its ability to modulate cellular responses. The nitrile group allows for further functionalization, enabling the creation of diverse derivatives for structure-activity relationship studies. Commonly employed in medicinal chemistry for optimizing drug candidates with improved metabolic stability and binding affinity.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,780.00
inventory 1g
10-20 days ฿5,760.00

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1H-Pyrrolo[2,3-c]pyridine-4-carbonitrile
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Used in pharmaceutical research as a key intermediate in the synthesis of kinase inhibitors, particularly for targeted cancer therapies. Its structure supports the development of compounds with high selectivity toward specific signaling pathways involved in tumor growth. Also explored in the design of anti-inflammatory agents due to its ability to modulate cellular responses. The nitrile group allows for further functionalization, enabling the creation of diverse derivatives for structure-activity relati

Used in pharmaceutical research as a key intermediate in the synthesis of kinase inhibitors, particularly for targeted cancer therapies. Its structure supports the development of compounds with high selectivity toward specific signaling pathways involved in tumor growth. Also explored in the design of anti-inflammatory agents due to its ability to modulate cellular responses. The nitrile group allows for further functionalization, enabling the creation of diverse derivatives for structure-activity relationship studies. Commonly employed in medicinal chemistry for optimizing drug candidates with improved metabolic stability and binding affinity.

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