tert-Butyl 2-(((6-(cyclopropylamino)pyrimidin-4-yl)amino)methyl)piperidine-1-carboxylate

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Reagent Code: #87309
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CAS Number 1353956-33-8

science Other reagents with same CAS 1353956-33-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 347.46 g/mol
Formula C₁₈H₂₉N₅O₂
badge Registry Numbers
MDL Number MFCD21098725
inventory_2 Storage & Handling
Storage Room temperature, sealed, dry

description Product Description

This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of biologically active molecules. Its structure, featuring both piperidine and pyrimidine moieties, makes it a valuable building block for developing potential drug candidates, particularly in the design of kinase inhibitors. These inhibitors are often explored for their therapeutic applications in treating various diseases, including cancer and inflammatory disorders. Additionally, the presence of the cyclopropylamino group enhances its ability to interact with specific biological targets, contributing to its role in optimizing drug potency and selectivity. Researchers also leverage its chemical properties to study structure-activity relationships (SAR) in drug discovery programs.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿10,665.00

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tert-Butyl 2-(((6-(cyclopropylamino)pyrimidin-4-yl)amino)methyl)piperidine-1-carboxylate
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This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of biologically active molecules. Its structure, featuring both piperidine and pyrimidine moieties, makes it a valuable building block for developing potential drug candidates, particularly in the design of kinase inhibitors. These inhibitors are often explored for their therapeutic applications in treating various diseases, including cancer and inflammatory disorders. Additionally, the presence of the cyclopropylamino group enhances its ability to interact with specific biological targets, contributing to its role in optimizing drug potency and selectivity. Researchers also leverage its chemical properties to study structure-activity relationships (SAR) in drug discovery programs.
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