2-(Phenyl)-4-(3-hydroxy-4-chlorophenyl)-5-(4-pyridyl)-1H-imidazole

98%

Reagent Code: #224908
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CAS Number 303727-31-3

science Other reagents with same CAS 303727-31-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 347.80 g/mol
Formula C₂₀H₁₄ClN₃O
badge Registry Numbers
MDL Number MFCD12828750
thermostat Physical Properties
Boiling Point 579.8±50.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.335±0.06 g/cm3(Predicted)
Storage 2-8°C, sealed, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Shows activity in modulating cellular signaling pathways involved in tumor growth and inflammation. Also employed in research settings to study apoptosis and cell cycle regulation. Its structure allows for strong binding to specific enzyme active sites, making it valuable in designing targeted therapies. Additionally, it serves as a building block in the preparation of fluorescent probes for biochemical imaging due to its conjugated aromatic system.

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Size Availability Unit Price Quantity
inventory 10mg
10-20 days ฿2,660.00
inventory 25mg
10-20 days ฿3,630.00
inventory 100mg
10-20 days ฿10,470.00

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2-(Phenyl)-4-(3-hydroxy-4-chlorophenyl)-5-(4-pyridyl)-1H-imidazole
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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. Shows activity in modulating cellular signaling pathways involved in tumor growth and inflammation. Also employed in research settings to study apoptosis and cell cycle regulation. Its structure allows for strong binding to specific enzyme active sites, making it valuable in designing targeted therapies. Additionally, it serves as a building block in the prep

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Shows activity in modulating cellular signaling pathways involved in tumor growth and inflammation. Also employed in research settings to study apoptosis and cell cycle regulation. Its structure allows for strong binding to specific enzyme active sites, making it valuable in designing targeted therapies. Additionally, it serves as a building block in the preparation of fluorescent probes for biochemical imaging due to its conjugated aromatic system.

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