N-(Pyrimidin-5-ylmethyl)pyridin-2-amine

95%

Reagent Code: #215598
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CAS Number 1383916-51-5

science Other reagents with same CAS 1383916-51-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 186.21 g/mol
Formula C₁₀H₁₀N₄
badge Registry Numbers
MDL Number MFCD24445664
thermostat Physical Properties
Boiling Point 360.1±22.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.247±0.06 g/cm3(Predicted)
Storage Room temperature, light-proof, 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 therapy. It serves as a building block in medicinal chemistry due to its ability to engage in hydrogen bonding and π-π interactions, enhancing binding affinity to target proteins. Also employed in the preparation of biologically active molecules targeting inflammatory and neurological disorders. Its structural features make it suitable for optimizing drug-like properties in lead compounds. Additionally, it is used as a ligand in coordination chemistry to study the properties of metal complexes.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿10,050.00
inventory 250mg
10-20 days ฿17,070.00
N-(Pyrimidin-5-ylmethyl)pyridin-2-amine
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Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer therapy. It serves as a building block in medicinal chemistry due to its ability to engage in hydrogen bonding and π-π interactions, enhancing binding affinity to target proteins. Also employed in the preparation of biologically active molecules targeting inflammatory and neurological disorders. Its structural features make it suitable for optimizing drug-like propertie

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer therapy. It serves as a building block in medicinal chemistry due to its ability to engage in hydrogen bonding and π-π interactions, enhancing binding affinity to target proteins. Also employed in the preparation of biologically active molecules targeting inflammatory and neurological disorders. Its structural features make it suitable for optimizing drug-like properties in lead compounds. Additionally, it is used as a ligand in coordination chemistry to study the properties of metal complexes.

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