N-((1H-Benzo[d]imidazol-2-yl)methyl)-1-(pyridin-2-yl)-N-(pyridin-2-ylmethyl)methanamine

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Reagent Code: #215593
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CAS Number 345349-15-7

science Other reagents with same CAS 345349-15-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 329.4 g/mol
Formula C₂₀H₁₉N₅
badge Registry Numbers
MDL Number MFCD31692663
thermostat Physical Properties
Boiling Point 543.0±45.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.269±0.06 g/cm3(Predicted)
Storage Room temperature, seal, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors for cancer therapy. Exhibits strong metal-chelating properties, making it valuable in catalysis for organic transformations such as cross-coupling reactions. Also employed in the design of fluorescent probes for detecting metal ions in biological systems due to its ability to bind selectively with transition metals. Its structural features support use in coordination chemistry for creating metal-organic frameworks (MOFs) with potential applications in sensing and catalysis.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿13,010.00
inventory 250mg
10-20 days ฿22,110.00

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N-((1H-Benzo[d]imidazol-2-yl)methyl)-1-(pyridin-2-yl)-N-(pyridin-2-ylmethyl)methanamine
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Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors for cancer therapy. Exhibits strong metal-chelating properties, making it valuable in catalysis for organic transformations such as cross-coupling reactions. Also employed in the design of fluorescent probes for detecting metal ions in biological systems due to its ability to bind selectively with transition metals. Its structural features support use in coordination chemistry for cr

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors for cancer therapy. Exhibits strong metal-chelating properties, making it valuable in catalysis for organic transformations such as cross-coupling reactions. Also employed in the design of fluorescent probes for detecting metal ions in biological systems due to its ability to bind selectively with transition metals. Its structural features support use in coordination chemistry for creating metal-organic frameworks (MOFs) with potential applications in sensing and catalysis.

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