1-(6-Ethoxy-pyrimidin-4-yl)-piperidin-3-ylaminehydrochloride

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Reagent Code: #184954
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CAS Number 1185319-56-5

science Other reagents with same CAS 1185319-56-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 258.748 g/mol
Formula C₁₁H₁₉ClN₄O
badge Registry Numbers
MDL Number MFCD09877729
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used in pharmaceutical research as a key intermediate in the synthesis of kinase inhibitors, particularly for targeting tyrosine kinases involved in cancer cell signaling. Shows potential in the development of targeted therapies for oncology, especially in compounds designed to inhibit tumor growth and proliferation. Also utilized in the creation of novel drug candidates due to its ability to enhance binding affinity and selectivity toward specific enzyme targets. Its structure supports optimization of pharmacokinetic properties in drug design, making it valuable in medicinal chemistry for improving metabolic stability and bioavailability.

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

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1-(6-Ethoxy-pyrimidin-4-yl)-piperidin-3-ylaminehydrochloride
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Used in pharmaceutical research as a key intermediate in the synthesis of kinase inhibitors, particularly for targeting tyrosine kinases involved in cancer cell signaling. Shows potential in the development of targeted therapies for oncology, especially in compounds designed to inhibit tumor growth and proliferation. Also utilized in the creation of novel drug candidates due to its ability to enhance binding affinity and selectivity toward specific enzyme targets. Its structure supports optimization of p

Used in pharmaceutical research as a key intermediate in the synthesis of kinase inhibitors, particularly for targeting tyrosine kinases involved in cancer cell signaling. Shows potential in the development of targeted therapies for oncology, especially in compounds designed to inhibit tumor growth and proliferation. Also utilized in the creation of novel drug candidates due to its ability to enhance binding affinity and selectivity toward specific enzyme targets. Its structure supports optimization of pharmacokinetic properties in drug design, making it valuable in medicinal chemistry for improving metabolic stability and bioavailability.

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