N-(pyrimidin-4-yl)acetamide

≥95%

Reagent Code: #216924
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CAS Number 16166-22-6

science Other reagents with same CAS 16166-22-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 137.14 g/mol
Formula C₆H₇N₃O
badge Registry Numbers
MDL Number MFCD18823812
thermostat Physical Properties
Melting Point 203 °C
inventory_2 Storage & Handling
Density 1.258±0.06 g/cm3(Predicted)
Storage Room temperature

description Product Description

Used in pharmaceutical research as a building block for synthesizing biologically active compounds. It serves as a key intermediate in the development of kinase inhibitors, which are important in cancer therapy. Its structure mimics purine bases, allowing integration into molecules that interact with enzymes and receptors involved in cell signaling. Also explored in agrochemicals for designing new pesticides due to its stability and hydrogen-bonding capability. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies to optimize drug candidates.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿17,580.00

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N-(pyrimidin-4-yl)acetamide
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Used in pharmaceutical research as a building block for synthesizing biologically active compounds. It serves as a key intermediate in the development of kinase inhibitors, which are important in cancer therapy. Its structure mimics purine bases, allowing integration into molecules that interact with enzymes and receptors involved in cell signaling. Also explored in agrochemicals for designing new pesticides due to its stability and hydrogen-bonding capability. Commonly employed in medicinal chemistry fo

Used in pharmaceutical research as a building block for synthesizing biologically active compounds. It serves as a key intermediate in the development of kinase inhibitors, which are important in cancer therapy. Its structure mimics purine bases, allowing integration into molecules that interact with enzymes and receptors involved in cell signaling. Also explored in agrochemicals for designing new pesticides due to its stability and hydrogen-bonding capability. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies to optimize drug candidates.

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