3,4-Dihydroimidazo[4,5-b]pyridin-5-one

≥95%

Reagent Code: #175684
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CAS Number 28279-48-3

science Other reagents with same CAS 28279-48-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 135.12 g/mol
Formula C₆H₅N₃O
badge Registry Numbers
MDL Number MFCD20037391
thermostat Physical Properties
Boiling Point 593.1±50.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, dry seal

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 supports binding to enzyme active sites, making it valuable in designing drugs that target specific signaling pathways in tumor cells. Also employed in research for central nervous system agents due to its ability to cross the blood-brain barrier. Commonly found in medicinal chemistry workflows for optimizing lead compounds with improved potency and selectivity.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿22,580.00

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3,4-Dihydroimidazo[4,5-b]pyridin-5-one
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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 supports binding to enzyme active sites, making it valuable in designing drugs that target specific signaling pathways in tumor cells. Also employed in research for central nervous system agents due to its ability to cross the blood-brain barrier. Commonly found in medicinal chemistry workflows for optimizing lead compounds with improved potency

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Its structure supports binding to enzyme active sites, making it valuable in designing drugs that target specific signaling pathways in tumor cells. Also employed in research for central nervous system agents due to its ability to cross the blood-brain barrier. Commonly found in medicinal chemistry workflows for optimizing lead compounds with improved potency and selectivity.

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