N,N-Dimethyl-N´-piperidin-4-yl-pyrimidine-4,6-diaminehydrochloride

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Reagent Code: #219613
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CAS Number 1185320-13-1

science Other reagents with same CAS 1185320-13-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 257.763 g/mol
Formula C₁₁H₂₀ClN₅
badge Registry Numbers
MDL Number MFCD12547735
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used in pharmaceutical research as a key intermediate in the synthesis of biologically active compounds, particularly in the development of kinase inhibitors. Shows potential in medicinal chemistry for targeting signaling pathways involved in inflammatory diseases and cancer. Also employed in the design of selective receptor antagonists due to its ability to cross cell membranes and interact with central nervous system targets. Its structure supports high binding affinity and improved metabolic stability in drug candidates.

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Size Availability Unit Price Quantity
inventory 500mg
10-20 days ฿28,410.00

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N,N-Dimethyl-N´-piperidin-4-yl-pyrimidine-4,6-diaminehydrochloride
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Used in pharmaceutical research as a key intermediate in the synthesis of biologically active compounds, particularly in the development of kinase inhibitors. Shows potential in medicinal chemistry for targeting signaling pathways involved in inflammatory diseases and cancer. Also employed in the design of selective receptor antagonists due to its ability to cross cell membranes and interact with central nervous system targets. Its structure supports high binding affinity and improved metabolic stability

Used in pharmaceutical research as a key intermediate in the synthesis of biologically active compounds, particularly in the development of kinase inhibitors. Shows potential in medicinal chemistry for targeting signaling pathways involved in inflammatory diseases and cancer. Also employed in the design of selective receptor antagonists due to its ability to cross cell membranes and interact with central nervous system targets. Its structure supports high binding affinity and improved metabolic stability in drug candidates.

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